About Us
Clinical Research Fastrack is the first training program to offer bootcamp-style, immersive Clinical Research curriculum with career coaching. Learn more about how we are transforming this industry!
Find Your Passion
Career Mentorship
Admissions
Instructors
DAVID SILBERMAN
Co-Founder and CEO
Clinical Research Fastrack
MEET THE TEAM
Advisory Board
Jay “Shoobie” Shubrook, DO FAAFP, FACOFP
Diabetes Researcher, Professor at Touro University
Dr. Shubrook is a Professor in the Primary Care Department at Touro University California. He also serves as the Director of clinical research at the College of Osteopathic Medicine. He has more than 15 years of research experience in clinical trials. As an investigator, he initiated research at Touro University. At Ohio University he served as Director of the Clinical Division at the Diabetes Institute at the Ohio University Heritage College of Osteopathic Medicine (OU-HCOM) and Director of the University Medical Associates Diabetes/Endocrine Cente, both in Athens, OH. Dr. Shubrook serves as an associate editor of The Journal of the American Osteopathic Association (JAOA) His personal research focuses on early intervention in type 2 diabetes and improving care for people with diabetes. Dr. Shubrook characterizes himself as a “curious scientist. Every day I have more questions. The balance in my job allows me to see patients-which is why we do all of this work-generate more questions, and go research these topics. Then I can share what we learned with patients, students and professionals which is very satisfying.”
Nancy Lizzul, RN
Associate Director Clinical Operations at PCM TRIALS - Quality Mobile Research
With over 20 years of healthcare and administrative experience I can provide an exceptional research experience through efficient, comprehensive support to the clinical practice and investigator while delivering safe and quality care to the patient. I have demonstrated the ability to effectively coordinate, lead, manage, monitor, educate, promote positive change, and provide supportive collaboration within clinical departments and organizations. I contribute to the success organizations by partnering with physicians, industry and administration to maintain all aspects of operations and continuance of best practice for clinical departments and patients. Through effective and consistent leadership, I have successfully developed teams who have provided new possibilities and hope for patients and families.
Mark Hanley
Advisory Board Member
Mark Hanley is a visionary in the healthcare industry who has dedicated his career to improving the quality of care across multiple disciplines. With a long history contributing to the clinical trial industry, Hanley has served as the Chief Executive Officer of Radiant Research, which he built into the country’s largest wholly-owned network of clinical trial sites. More recently he has served as CEO of VirTrial, a ground-breaking telehealth platform provider for decentralized trials. In addition, he is the past CEO of The Society of Clinical Research Sites (SCRS). Hanley’s career positions have all supported his goal in improving access to clinical trials.Mark has also been a consultant to numerous companies in the healthcare industry, an Independent Director of Allied Healthcare International Inc., Stratus Video, as well as ZVRS, an industry leader in communication access services, and is past Chairman of the Board at StudyKIK, a patient recruitment provider for the clinical trials sector.
David Silberman
Co-Founder & CEO
David Silberman is the CEO and Founder of Clinical Research Fastrack and a seasoned health education entrepreneur who has created and operated educational programs and non-profit organizations in Arizona, Texas, and California. David has the unique ability to develop strong organizations and construct vibrant communities. As a founder of National Laser Institute, David helped build this company into the largest medical aesthetics training center in the United States. At Clinical Research Fastrack his focus is on offering an engaging curriculum delivered by a team of experts who serve as passionate and knowledgeable instructors. Before founding National Laser Institute and Clinical Research Fastrack, David held executive level positions at Health Ventures International in Scottsdale, AZ and at educational non-profit organizations in the San Francisco Bay Area. He earned his BA in Politics from the University of California, Santa Cruz, and a Master’s Degree in Public Health from the University of California, Los Angeles. In addition to his professional career, David has served as a community volunteer in which he presided as the Chair of the Board of Directors for the I Have a Dream Foundation-San Francisco. In one of his most challenging and rewarding volunteer roles he served as PTO Co-chair at his children’s elementary school where he helped to transform the school into one of the most sought after elementary schools in San Francisco.
Louis Silberman
Co-Founder & Chairman
Louis J. Silberman, the Co-founder and Board Chairman of Clinical Research Fastrack, is known for pioneering the medical aesthetics training industry over a decade ago with his vision to create National Laser Institute. National Laser Institute trains physicians, nurses, aestheticians, and career-changers in cosmetic lasers, cosmetic injections and anti-aging treatments. Silberman was the first to market reinventing the medical aesthetics education space with short intensive programs. He grew National Laser Institute to be nationwide, providing training in Scottsdale, Dallas, Chicago, Boston, Philadelphia, Denver, Las Vegas, Nashville, San Francisco, Beverly Hills and Newport Beach. Silberman partners with Allergan (AGN on the NYSE) and works closely with many publicly held laser companies who support National Laser Institute’s training programs. As the industry for medical aesthetic training has grown with hundreds of competing programs, National Laser Institute is now held as the gold standard in the industry for quality and excellence, and attendees fly in from across the globe to receive training at National Laser Institute. National Laser Institute also operates medspas within its educational facilities. This national training institute sees up to 3,000 clients per month. Louis Silberman was also a semi-finalist for the 2014 Ernst and Young Entrepreneur of the Year Award (prior award recipients include the founders of Google, Starbucks, Southwest Airlines, Dell, and Amazon). He is also known for starting Health4her.com, a women’s health and beauty retailer. Louis is a published author and nationally recognized medical aesthetics training expert, and a contributing editor for some of the country’s largest skin publications, including Skin Inc., Dermascope and Les Nouvelle. He is both an industry and motivational speaker at large venues nationwide. Louis has been written about in many publications including Entrepreneur Magazine, Business 99, The Business Journal, Internet Retailer, Woman’s World, E-merging Business, The Arizona Republic, Skin Inc., and Fortune Small Business.
Career Mentorship Team
Ian Fetterolf
Career and Outreach Coach
Ian brings inclusivity, positivity, and motivation to participants with 10 years+ experience through 21st-century skill immersion and hands-on credential/experience building workshops / curriculum. His teaching/training focus includes workforce development, career development, high school equivalency education, life skills training, software technology, business processes, and marketing.
Julia Martin
Head of Career Services
Originally born and raised on the coast of Maine! I have an educational background in Social Work and Psychology. I have 5+ years of experience in Career Coaching utilizing a strength-based, solution-focused strategy to support a broad range of diverse individuals, adults, young adults & youth, in overcoming any obstacles they may be facing in achieving their ultimate career goals. I am incredibly passionate about supporting others in turning on their own unique light and come into undeniable confidence that will allow them to step into their greatest potential.
Moné Brown
Education Coordinator
Mone’ Brown has been with Clinical Research FastTrack since February 2021 and has over 12 years of Clinical Research experience. She has her Bachelors in Health Science and a Masters in Regulatory Science and Psychology from Johns Hopkins. She started her career in the industry as a Research Assistant in 2006 at a small clinic that specialized in Rheumatoid Arthritis before accepting a position with a Pharmaceutical company in 2012 as a Regulatory Document Specialist. Within her role at Amphastar Pharmaceuticals she performed duties from Study Start-Up to Close Out, creating Informed Consent and Assent forms, Phase I – Phase IV IRB Submissions as well as IND submissions, and NDA submissions to FDA, managed document control, edited study reports, and performed internal audit tasks. She has also worked as a Regulatory Specialist for Kaiser Permanente Research and the most recent Covance known now as Labcorp Drug Development. She has worked on a very wide range of therapeutic areas within her Clinical Research career. In her personal time, Mone’ enjoys spending time with her family, as well as being very adventurous and riding extreme Rollercoasters, skydiving, traveling, singing, and mentoring those who want to enter into Clinical Research. Mone’ has a passion for Clinical Research and truly loves knowing that she’s making a difference and impacting so many lives.
Genielle Rodriguez-Brewer
Director of Education
Genielle has her Bachelor’s in Public Health Education and Promotion and has been working as a Clinical Research Coordinator since 2016. She was certified with the Association of Clinical Research Professionals in 2019 which led her to run multiple clinical research sites and even represent the U.S. as a National Study Coordinator for a leading pharmaceutical company. Her knowledge and experience developed into a passion for mentoring others into the research field in hopes to continue to make a difference.
Lauren Ballina Chang
VP of Strategic Growth
Lauren is a leading educator in clinical research who gained her experience conducting clinical trials at the Mayo Clinic as well as overseeing longitudinal studies at UNC’s trauma center. She earned her degree in Psychology and Latin from the University of South Carolina. She also has her Master’s in Biomedical Science from Midwestern University.
Admissions Team
Rachel Butler
Admissions Representative
Rachel is a medical professional with a Bachelor's degree in nursing and a heart for serving the medical community. She has experience working in inpatient and outpatient settings, specifically caring for surgical patients. She currently resides in Arizona. She is excited about getting people involved in medical research to improve quality of life in patients and medical professionals.
Noah Hargett
Senior Admissions Representative
Noah was born and raised in the Pacific Northwest before graduating from Liberty University with a B.S. in Religion. He has worked in a variety of industries including finance, manufacturing, and higher education. Noah is passionate about people, thrives on building relationships, and loves to help others become the best version of themselves. His hobbies include traveling, reading, and staying active.
Debra Giuffre
Senior Admissions Representative
A native of Honolulu, Hawaii, Debbie came to the continental United States to attend Michigan State University, where she graduated with a degree in Hotel and Restaurant Management. After college she went on to work for Marriott International in California. Later, Debbie moved to Phoenix, Arizona, to complete a court reporting degree, and went on to work within the courtroom industry for several years. Debbie’s strong background in hospitality and relationship building, coupled with her passion for the possibilities presented by the clinical research field led her to joining our team. Her strong commitment to helping others, has fueled her desire to see a cure for Dementia/Alzheimer’s within her lifetime. Outside work, Debbie loves to cook, read, hike, spend time with her two sons, and walk her Great Dane, Sam.
David Schillne
Senior Admissions Representative
David has an incredible passion for helping students and professionals achieve their academic and career goals. He holds an undergraduate degree from the University of Arizona, while his post-graduate studies culminated in earning his MBA. His 20-year career includes roles as Director of College Admissions and Vice President of Recruiting. Academically, David has personally assisted hundreds of U.S. and foreign students in earning full ride and six-figure scholarships to such prestigious schools including Stanford, Vanderbilt, Carnegie Melon, Purdue, Xavier and Occidental. Professionally, David understands how challenging the process has become to begin a career in clinical research. Through our program at Clinical Research Fastrack, he helps recent college graduates and those “re-careering” to successfully navigate this new landscape. Some of the companies that David’s students are now enjoying incredible careers include: The Mayo Clinic, Covance, Synexus/Radiant Research, Jean Brown Research, Phoenix Children’s Hospital, UT Southwestern Hospital, Baylor Scott & White Health, Scottsdale Medical Imaging and Keystone Research. He looks forward to helping your career dreams in clinical research become a reality.
Anthony Huff
Director of Admissions
Anthony has been an admissions leader with Clinical Research Fastrack since 2021. He loves working with people and finding ways to inspire others to reach their goals. He enjoys time with his family, traveling, and self-development. Anthony graduated from the University of Arizona.
Operations Team
Kyera Tate
Communications Associate
Kyera is a young mother of 2 who currently resides in California. Her background has a unique blend of expertise in social work and laboratory science, Kyera brings a multidisciplinary approach to addressing complex issues in healthcare and community well-being. Holding a Bachelor's degree in Psychology and a Certificate in Laboratory Science, Kyera has cultivated a diverse skill set that bridges the gap between clinical research and social support.
Sarah Hargett
Director of Operations
Sarah, a native of the Pacific Northwest, brings a wealth of experience in operations, payroll and administrative support to her professional endeavors. Her true passion lies in working collaboratively to help students achieve their academic aspirations. Beyond her career, Sarah enjoys traveling and savoring diverse culinary experiences with friends and family, cherishing the value of relationships in her life.
Courtney Herman
Class and Communications Coordinator
Courtney is a Class and Communications Coordinator at Clinical Research Fastrack. Helping people and trying to make a difference are among the many things she is passionate about. She enjoys taking her husband and kids on adventures as often as possible. When she's not at work, you can find her watching scary movies and crime shows or hanging out with family.
Tamara Langston
HR Associate & Communications Manager
Tamara Langston I am the Human Resource Associate at Clinical Research Fastrack. Tamara was born and raised in Southern California. Tamara has a strong background in Health care, Psychology, and Behavior Analysis with a passion for making change. Tamara's hope is to continue to change the lives of others and continue to grow in the field of science. Working at Clinical Research Fastrack she has been able to meet those goals by helping students looking for a career change.
Creative Team
Benjamin Bosler
Content Creator
Ben currently resides in Fayetteville, Arkansas, where he attended the University of Arkansas and earned a bachelors in communication. He hopes to make a difference in people's lives and share inspiring messages in his work. In his free time, Ben likes to spend time with friends and watch movies with his three-legged cat, Liza.
Instructors
Joy Geallis
Instructor
Joy Geallis joined Immunitas in March 2021 as the head of clinical operations and brings a decade of experience in the pharmaceutical industry. Prior to joining Immunitas, Joy was the director of clinical trial operations and monitoring at Xeris Pharmaceuticals in Chicago. In her time at Xeris, Joy developed and implemented clinical development strategy for multiple programs starting from pre-clinical through to new drug application, or NDA, filing. She has extensive experience in the clinical space building strategic processes to deliver on clinical timelines and build relationships with internal and external stakeholders in the drug development process including interactions with regulatory bodies and academic institutions.
Carlos Orantes
Instructor
Current CEO, Alcanza Clinical Research. Over 30 years of experience in the drug development industry ranging from the pre-clinical sector through late stage clinical space. This includes senior executive management roles for large and small, private and publicly held entities, as well as domestic and international companies.
Zoé Felicié
Instructor
Current Sr. Patient Diversity Specialist, PPD. Energetic and adaptable clinical research professional with over a decade of research experience. I’m truly passionate about diversity, equity, inclusion and belonging. In my current role I’m able to leverage my past experiences in Clinical Research which include patient recruitment and retention of diverse patient populations, community engagement, cultural competency training and education.
Ashley Moultrie
Instructor
Current Senior Director, DEI & Community Engagement, Javara. Certified Clinical Research Professional with over ten years of industry experience; dedicated to eliminating health disparities and making clinical research information and opportunities accessible to ALL patients, with an intentional focus on underrepresented and underserved communities.
Andrew Adorboe
Instructor
Current System Director and Research Compliance Officer, Tower Health. I am a dynamic research compliance leader with the clarity of vision forged from over 15 years in research compliance and administration in large healthcare settings with a demonstrated history in strategic compliance activities, built sustainable research compliance programs from scratch, delivering on human and institutional protections, RCR-responsible conduct of research, research misconduct and experienced in IRB, biosafety, export control, sponsored programs, and healthcare quality improvement. I am focused on delivering impactful values to my institution.
Dan Otap
Instructor
Current Principal, Alliance and Partnerships Lead, Genentech. I have cultivated a deep understanding of regulatory standards, compliance requirements, and the intricacies of human subjects research and clinical operations. My specialization lies in optimizing site operations with Sponsor relationships and ensuring efficient bi-directional execution.My aim is to act as a connector between various stakeholders within the clinical research ecosystem, fostering collaborative relationships between Sponsor developmental sciences, translational sciences, clinical science, clinical operations, CROs, Solutions providers, and site leadership. I aspire to be a thought leader in this space, leading discussions and shaping best practices in the management of Sponsor/CRO/Site relationships.
Kathy Mickel
Instructor
Current Learning Solutions Leas, SCRS. Over the course of my career and volunteer engagements, I've successfully tackled diverse projects across various industries, working with multifaceted populations. This breadth of experience has honed my skills in problem-solving, learning agility, adaptability, and both operational and strategic project management.My professional journey has equipped me with extensive experience navigating matrix organizations, overseeing field-based teams, and delivering results in dynamic environments. With a track record of contributing to organizational transformations, I specialize in driving process improvements that optimize resource allocation, foster financial growth, boost productivity, and enhance overall capabilities.
Kristin Surdam
Instructor
Certified (CCRC & PMP) clinical research professional with almost 20 years in the industry, currently responsible for the Thought Leadership and Strategy team at Florence Healthcare, a digital health company that streamlines clinical trials.My mission is to drive clinical research forward through cross-industry collaboration, innovation, and quality. I have demonstrated therapeutic expertise in oncology, CNS, and other areas, as well as proficiency in all aspects of clinical trial management, from concept to completion. I have successfully delivered multiple multi-center, phase I-IV clinical trials, at both the site and sponsor levels, with timely and efficient outcomes.
April Bell
Instructor
Current Manager, Clinical Research Operations, JPS Health Network. Certified Clinical Research professional qualified by over 20 years of achievements as a research coordinator, educator and manager. Combine resourcefulness and problem solving skills with clinical trial knowledge to consistently deliver accurate and efficient results. Dedicated to quality and continuous improvement.Knowledge in all areas of research including contracting, budgeting, ICH-GCP, IRB protocol submissions, renewals and on-going regulatory documentation including safety reporting. Demonstrated competencies in managing clinical trials data, formulating source documents, AE/SAE reporting and developing & maintaining excellent sponsor relationships. Able to manage multiple responsibilities without compromise to detail or quality.
Michele McMahan Meek
Instructor
Current Senior Manager, Clinical Operations at Thermo Fisher/PPD. Efficient, motivated senior manager with more than 19 years’ experience in clinical operations; including, People/Line Manager, RBM Lead, Clinical Trail Manager and CRA. I have experience within the Pharmaceutical space as well as CRO (FSP and multi-Client model), so I am knowledgeable on varied ways of working.
Stephen Ramirez
Instructor
CEO at Atlantic Medical Research. Results-focused clinical research professional with strengths in clinical study management, regulatory compliance, patient care, and study-team collaboration. Proficient in clinical trial conduct and multidisciplinary teamwork to promote quality and productivity in meeting study timelines and milestones while ensuring patient safety. Adept at managing concurrent objectives to promote efficiency and influence positive outcomes.
Mary Sophy Yohannan
Instructor
Mary Yohannan is an International Medical Graduate with 18 years' experience in Clinical Research over several therapeutic areas, including Gynecology, Oncology, and Cardiology. She has worked as a phone screener, data manager, clinical research assistant, certified coordinator, manager, CRA, and is currently a Clinical Evaluation Scientist. Mary has screened, consented, and enrolled patients, negotiated budgets, written grant applications, compassionate use requests, consent forms, protocols, abstracts, and papers. She has also been involved in Sponsor and FDA audits and responded to a 483 warning letter. Now she collects evidence to report on safety and performance of medical devices. Over the years she has recognized the need for strong guidance and mentorship as new professionals enter the field.
Erin Davis
Instructor
After 5 years at Winship, Erin is now the Clinical Project Manager at IQVIA. Erin has been in the clinical research industry for almost 13 years, spending 12 of those years working in Oncology. She highly enjoys working on the site side, seeing the positive impact of treatments, in the lives of patients. She recently started working in operations, providing her a different view and experience of the industry; with aspirations of being a site Director one day. She currently lives and works in the Atlanta area, spending the majority of her time with her fur babies, Raja and Meeko. She also enjoys time outdoors, traveling and occasionally, a night in, watching something Marvel.
Heather Diederich
Instructor
Heather Diederich is the Director of Operations for CCT Research with over 16 years experience in the research industry. Prior to becoming a Director of Operations, she coordinated clinical trials for 13 years and has been a finalist for "Researcher of the Year- the America's" by PharmaTimes Magazine in 2016, 2017, and 2018. Heather is committed to the overall success of all trials. With her strong desire and extensive clinical research knowledge that she has gained from conducting over 160 successful trials, she loves that she has the opportunity to help improve the advancement of medicine.
Deena Bernstein
Instructor
Deena Bernstein has deep expertise in healthcare leadership and the clinical research industry. Her career spans over twenty years in clinical research site development, operations and digital technology for the clinical research industry. Deena is a passionate leader with an entrepreneurial spirit that cares deeply about improving the clinical trial experience and process for study participants. She thrives on innovation and is the VP of Customer Success at Datacubed Health. She focuses on delighting customers, patient engagement & retention, decentralized clinical trial models, Site training models that reduces burden, and clinical research as a care option. She looks at her role as the Ambassador to Happiness.
Russell Herstein
Instructor
Clinical research professional with nearly 20 years of industry and academic clinical research experience in all aspects of clinical trials from feasibility to close out. Background experience in phase 1-4 studies with multiple indications including: neurological sciences, oncology, vaccines, gastrointestinal, cardiology, dermatology, pulmonary, diabetes/endocrine, and pediatric trials. Foundation continually built on deep-rooted quality, and team-first attitude. Emphasizes best practices at site and operational levels to strengthen efficiency and productivity while growing and maintaining established relationships - both internal and external. During my tenure as Site Director during the COVID-19 pandemic, our site grew from 10 FTE to 27 FTE team members. Our site in northeast Nebraska was also the first site to successfully enroll a patient into the first Phase 2, mRNA, SARS-COV-2 vaccine trial in the country.
Mea Ebenbichler
Instructor
Mea Ebenbichler, BA, CCRC, ACRP-PM, CHRC-Quality Compliance Auditor is a Nationally Certified Clinical Research Professional with over 20 years of experience managing and coordinating clinical trials in Pediatric Lung Transplant, Bone Marrow Transplant and Oncology. Currently as the Quality Compliance Auditor for EmVenio Research she is ensuring clinical research compliance through proper support within the areas of human subject protection, clinical study conduct, and regulatory compliance. Oversees clinical research risk management, via monitoring and auditing, assuring proper data safety and biosafety compliance. Serves as an active member of the Quality and Compliance Committee. Before joining EmVenio Research she served as a Jr Research Integrity Officer (RIO), she reviewed and evaluated Public Health Service of the U.S. Department of Health and Human Services (PHS/HHS) funded institutions' compliance, as appropriate with PHS regulations. Conducted policy analyses, derived outcome assessments that informed and modernized the Office of Research Integrity’s approach to scientific compliance and identified opportunities for potential regulatory or procedural changes. Developed, recommended, and enforced HHS compliance actions in accordance with the PHS policies. Prior to transitioning into Quality Compliance, she developed the Pediatric Lung Transplantation Research Program at TCH/BCM with the direction of doctors Ernestina Melicoff, and George Mallory. They told her what they wanted and together they went onto publish several papers and presented at National and International conferences. Mea received her Bachelor of Arts with University and Departmental Honors in Psychology from Wayne State University and presently is a Juris Master-Compliance candidate at Liberty University School of Law. An active member of SOCRA, ACRP, PSI CHI, and volunteers with GirlTrek, the largest public health non-profit for African-American women and girls in the United States, Remote Area Medical which is a non-profit provider of mobile medical clinics delivering free dental, vision, and medical care to under-served and uninsured individuals, and Montrose Grace Place a safe space for vulnerable homeless youth.
Karimah White-Murphy
Instructor
Karimah White-Murphy is a certified research professional with The Society of Clinical Research Associates (SOCRA). She has over 12 years experience in clinical research and the pharmaceutical industry. After collaborating with a number of CROs and Pharma Sponsors, she made the decision to start KarMur, LLC, a company that specializes in short- and long-term contracts to aid CROs and Pharma Sponsors in achieving their objectives for clinical research.
Lauren Horton
Instructor
In her role as Division Director of Research, Dr Lauren Horton believes in equipping others with the tools they need to succeed. With her expertise, she has been able to successfully develop protocols, clinical designs and test strategies to assist in the development of research and product development projects. Prior to joining HCA Healthcare, she was the senior manager of scientific affairs at a leading nutraceutical company. Dr. Horton is passionate about improving the quality of life of those living in her community. Her passion for helping people led her to pursue a career in research, and through her work, she has become an advocate for equitable patient care as well as access to innovative research therapies. Dr. Horton holds a bachelor's degree in biology from Rust College, a master's degree in health economics and clinical outcomes research from Xavier University, and a doctorate in biomedical science from Morehouse School of Medicine. In addition to being the mother of two amazing children, Dr. Horton has two dogs, Sterling and Gracie Mae, and is married to Tim Horton, not to be confused with the popular Canadian coffee chain, although sometimes she wishes it was.
Maria Lavarreda-Pearce
Instructor
Maria Lavarreda-Pearce is a Sr. Research Analyst at a Community Hospital in the Central Coast of California. In her role, Maria oversees the feasibility and supports start-up activities for clinical trials. She leads initiatives and directs training and education sessions on research design and methodology to clinicians, faculty, and staff. Before devoting her work fulltime to clinical projects, Maria begun her research journey working on kidney and lung development research projects in the laboratories at the Saban Research Institute at Children’s Hospital Los Angeles. Maria’s passion to plan and execute research projects led her to focus on project management and transition to Research Operations to support research trainees across different career stages and at various academic levels.
Tiffany Ashton
Instructor
Tiffany Ashton, MAS, CCRA, is a seasoned Clinical Research Professional with over 20 years of experience. Tiffany has served various Clinical Research roles, including CRC, CRA, and CTM, and gained firsthand industry-specific expertise that is second to none. As the Director of Operations for ClinEssentials, Tiffany utilizes her experience to understand the daily pressures that research professionals face. In this role, she works to strategically address challenges, overcome obstacles, provide critical guidance, and sharpen skills to elevate careers to the next level. Connect with Tiffany on LinkedIn @tiffany-ashton-clinessentials. Learn more about ClinEssentials at https://clinessentials.com/
Dr. Leketa Hawkins
Instructor
Dr. Leketa Hawkins (Keel) received a Bachelor of Science in Biology and Chemistry along with a Masters of Healthcare Administration from Winston Salem State University. She also holds a Doctorate of Philosophy Degree from Trinity International University. Dr. Hawkins has been a In House CRA, traveling CRA, and CTM. She is currently the Manager of Clinical Operations at a Clinical Research Organization. Beyond her impactful roles, Dr. Hawkins is a two-time Amazon #1 Best Selling coauthor. She has also been featured on Business Innovators Podcast and actively engages with various professional Clinical Research organizations. She is also a Presidential Lifetime Achievement Award recipient awarded by the Biden-Harris Administration. Balancing her professional achievements, Dr. Hawkins finds joy in spending quality time with family and friends. She is married and resides in the Greater Triangle area.
Brianna Angulo
Instructor
Brianna is a seasoned research professional with over 13 years of comprehensive experience in clinical research. With a diverse background encompassing both onsite and remote roles, Brianna brings a wealth of knowledge and expertise to the field. Brianna is certified through the Association of Clinical Research Professionals (ACRP) and is active within the research community. Holding an undergraduate degree in public health and a graduate certificate in public health sciences, Brianna's academic foundation complements her practical experience seamlessly. She is finishing up a Master of Science in Clinical Research Management and is dedicated to staying at the forefront of industry advancements. As the owner of a successful research agency and as an independent clinical research contractor, Brianna is recognized for her professionalism, dedication, and passion for advancing medical research.
Mitchell Hilbe
Instructor
Mr. Hilbe began working in clinical research in 2005 and has had a career on multiple therapeutic areas. Mitchell has served in clinical operations leadership roles at CRO and Sponsor organizations with a focus on late phase clinical trials and expanded access programs and is the CEO/Co-Founder of a site management organization. He is also the founder of the Clinical Research Justice League and promotes innovation in research and healthcare equity.
Jess Thompson
Instructor
Passionate about Clinical Research Professionals' professional development and well-being, Jess founded the Clinical Research Project Manager Association (CRPM Association) to provide education, career opportunities, and a supportive community. CRPM Association is committed to addressing the unique challenges of clinical research professionals through tailored wellness initiatives, and empowering members both professionally and personally through training, networking, and professional development. Jess emphasizes viewing Clinical Research Professionals as whole individuals, fostering a culture of well-being beyond project delivery.
Melissa Cisneros
Instructor
Melissa is currently a Clinical CRA Manager and has 13+ years of clinical research experience, including in a PK lab setting for phase I studies. She also has experience in phase II - IIII studies as a Remote Site Monitor, CRA, CRA Trainer, and CRA manager. She has onboarded jr. CRAs for about 2.5 years now and enjoys supporting their growth and seeing them thrive. She works as a Clinical Manager for Pharmaceutical Product Development (PPD), a global CRO.
Anhaita Jamula
Instructor
Anhaita Jamula, CCRC, is the Director of the Research Program at EvergreenHealth, a Kirkland, WA-based health care system. A self-described science geek, Jamula brings the perfect balance of business acumen, patient-focused dedication, and clinical research expertise to her role. She has over 20 years of experience in research management and a resilient passion to continuously evolve EvergreenHealth’s research program with the ultimate vision to offer a clinical trial for every patient that comes to EvergreenHealth. Jamula is responsible for the business development, financial and contracting management, legal contracting activities, capital resourcing, regulatory compliance and operations across the entire Research Program. As Director, she has successfully implemented a new business plan to improve business growth and optimize team infrastructure. A studied and accomplished leader, Jamula has learned and introduced Research Lean Methodologies, Change Mastery and Toyota Production System practices to her work, benefitting not only her work but also the work of her team and the lives of her patients. Jamula has led her team to facilitate sponsored clinical studies as well as internal investigator-initiated research programs across a spectrum of subjects, driven by the overarching goal to make clinical trial opportunities available to patients and families and to advance the health of the community.
Shirley Helm
Instructor
Shirley has worked in the clinical research ecosystem for several decades including managing a core research laboratory, conducting research participant testing, managing regulatory staff, development of ancillary service agreements, and currently oversees and directs the creation, development, and delivery of Education, Training and Resources for clinical research professionals. VCU’s post-baccalaureate certificate in clinical research (initiated Fall 2020) is one result of her efforts and she is now enrolled in this program! Shirley also is the Central VA SOCRA Chapter Chair and serves on the SOCRA certification exam question development committee.
Chizobam Obi
Instructor
Chizobam is a self-driven clinical research professional with a solid background in clinical research, project management, and supervision of clinical trials in accordance with ICH GCP guidelines. She is skilled in healthcare consulting, nursing and clinical research education, quality improvement, systems change analytics, and project management. Chizobam is passionate about mentoring future nurses and clinical research professionals and equipping them with the tools to succeed in their profession!
LaShawna Green
Instructor
LaShawna began her career as a clinical research coordinator in 2002 shortly after graduating with her Bachelor's Degree in Biology from the University of South Carolina-Columbia. After four years of working as at a clinical research coordinator at a busy Gastroenterology/Hepatology practice, she elected to further her education and graduated with her nursing degree in 2008. LaShawna continued to work as a registered nurse for four years before ultimately answering her calling to return back to clinical research as a clinical research nurse. Her nineteen years of clinical research experience spans across a number of specialties including interventional cardiology, valve & structural heart disease, cardiovascular sciences, hepatology, gastroenterology, drug & device trials. Over the past nine years, she has been working in the Texas Medical Center at healthcare system/academic institute as a clinical trials manager (RN) overseeing the daily operations for the divisions of Electrophysiology, Critical Care, and Valve & Structural Heart Disease. LaShawna is board certified in cardiovascular nursing from American College of Cardiovascular Nursing and a certified clinical research coordinator through Association of Clinical Research Professionals (ACRP) and President Elect for the local chapter of ACRP. She's an active member of International Association of Clinical Research Nurses (IACRN), 2021 Leadership Fellow Program and local chapter treasurer. In her free time, she enjoys travelling, reading, swimming, mentoring young research professionals, spending time with her husband & two toddlers and a host of family and friends. Welcome to a wonderful career in clinical research!
Portia Bowden
Instructor
Portia is currently the Patient Engagement Manager at Allucent. She was previously a Patient Recruitment Lead and works with Biotech & Pharma Companies in developing Global digital & traditional outreach strategies for clinical research studies. Portia promotes the importance of health literacy and patient advocacy within minority communities. She specializes in Rare Disease, Cardiovascular, Neurology, and Oncology Research.
Tiffany Drummond
Instructor
Over the last 15+ years, Tiffany developed her skills as a leading clinical research professional with career experience in coordinating trials, regulatory, program management, training, and medical writing! She has hired and mentored many in the field who have found success as CRAs, Project Managers, Clinical Research Coordinators, Data Managers, and more!Her professional and personal mission is to promote education in healthcare and science & research through instruction, speaking engagements, and social media platforms.
Chevy Brown
Instructor
Chevy Brown graduated from the University of South Carolina (in Columbia, SC) with a B.S. degree in Exercise Science and Master's Degree in Public Health, with an emphasis in Physical Activity in Public Health. Her career in clinical research began in 2007 as a research assistant at a stand-alone site in Greenville, SC. She had the opportunity to learn many roles while working in several departments there; this includes regulatory, data management, monitoring, budgets and contracts, laboratory, site management and staff training. In 2010, Chevy moved to Atlanta, GA to start, and subsequently manage, a total of 7 research sites. In 2019, Chevy became the Clinical Trials Manager for Irrimax Corporation, a small/medium-sized medical device company and was later promoted to Director of Clinical Trials. Chevy and her husband George currently reside in Duluth, GA with their 2 cats. In her spare time, Chevy enjoys teaching for Clinical Research Fastrack, reading fiction and history, watching The Golden Girls and practicing martial arts. She has a brown belt in American Kenpo Karate and is currently practicing Krav Maga.
RICHIE KAHN, MPH
Instructor
Richie is the Co-Founder and COO of Canary Advisors. He has been a Senior Director of Patient Success for Medable, Inc. Health policy professional by training; clinical researcher by trade; and patient advisor by necessity, Richie Kahn is intensely passionate about incorporating the passionate perspective to streamline clinical development and ultimately reduce the time it takes to bring promising new therapies to the patients that need them most.
WILLIAM JONES, BS, CCRP
Instructor
William Jones is the Chief Operating Officer at Epic Medical Research. He held the same role at Ventavia Research Group. William Jones, CCRP received his degree in Health Education Interdisciplinary Biology and Music from Texas A&M. William has worked in research since 2003. He has worked on numerous trials and enjoys sharing his passion and exuberance for helping advance medicine through research. In his spare time, he loves spending time with his wife and kiddos!
TERRI BURGHART, MBA
Instructor
Director of Operations at Pinnacle Clinical Research. Experienced Research Operations Director with a demonstrated history of working in the clinical research industry. Skilled in Sales, Good Clinical Practice (GCP), Biotechnology, Psychology, Pharmaceutical Industry, and Clinical Research. Strong medical practice and research manager with a Master of Business Administration (MBA) from University of South Florida, Certification of Medical Practice Executives from the Medical Group Management Association (MGMA), and a history of certification in clinical research (CCRC).
TASIA LONG, MS
Instructor
Tasia Long is currently the Project Manager II at Fortrea and was previously the Clinical Team Manager at PPD, part of Thermo Fisher Scientific. A dedicated Research Program Manager with over 14 years of experience overseeing and conducting clinical research studies to include: protocol design, planning and execution; data management; and contract/grant proposal and peer-reviewed literature writing in the specialty areas of emergency medicine/trauma, rheumatology, psychiatry, pulmonology, and pulmonary oncology. Highly skilled in project management and capable of delegating responsibility while leading a team, managing subcontractors, and maintaining timelines and budgets. An articulate collaborator who is capable of motivating a multi-institutional team to enhance efficiency and productivity.
SHANI HILLIARD, MS, CRM
Instructor
Shani is a Senior Associate at Amgen and is an experienced Clinical Project Manager with a demonstrated history of working in the hospital & health care industry. Skilled in Clinical Data Management, Clinical Research Experience, Business Development, and Critical Thinking. Strong program and project management professional with a Master of Science (MS) focused in Clinical Research Management from Arizona State University.
SEAN WALSH, MBA
Instructor
Experienced leader with a demonstrated history of working in the pharmaceutical and medical industry. Skilled in Clinical Operations, Patient Recruitment, Hospital Administration, and Public Speaking. Strong operational executive with a Master of Business Administration (M.B.A.) focused in Business Administration and Management.
SAM CHIMIENTI, BS
Instructor
Sam Chimienti is a Clinical Research Associate II at ICON Strategic Solutions and previously served as a Clinical Trials Compliance Analyst after serving as Senior Clinical Research Coordinator at Phoenix Children’s Hospital. Sam was born and raised in Chicago and moved out to Arizona in his teens. He graduated from Arizona State University with a Bachelor’s Degree in Kinesiology and worked for 5 years as a Clinical Research Coordinator before being offered an amazing opportunity to work with oncology patients at Phoenix Children’s Hospital. He is privileged to work alongside some of the top oncologists in the nation developing protocols for breakthrough drugs. He is also proud to have co-authored a pediatric oncology protocol. In his spare time, he likes to do yoga, hike, and try new restaurants.
SARAH HARVEY, BS
Instructor
Sarah Harvey is currently working as a Global Project Manager at Accelerated Enrollment Solutions. Her therapeutic areas of expertise include Cardiology, Women’s Health, Endocrinology, Gastroenterology, Genitourinary, CNS, and Vaccine. Sarah was born and raised in Maryland and moved to Arizona in 2012. She earned a Bachelor’s Degree in Sociology from Arizona State University. In her spare time, Sarah enjoys reading and spending time with her daughter.
RACHEL STANCL, MPA
Instructor
Clinical Research Project Manager at Dignity Health. Experienced Research Coordinator with a demonstrated history of working in the hospital & health care industry. Skilled in Phlebotomy, First Aid, Cardiopulmonary Resuscitation (CPR), Healthcare, and Basic Life Support (BLS). Strong research professional with a BS focused in Biology from ASU.
MEHA SHARMA, MS-CRM, CCRP
Instructor
Meha Sharma is the Clinical Country and Site Lead at Biogen. She was previously a Senior Associate Study Manager and is a Clinical Research Educator. Meha has been an instructor at Clinical Research Fastrack, since 2016. In her spare time, Meha enjoys traveling and being outdoors.
MARIA MARTIN, BSBA
Instructor
Maria is a Clinical Research Associate at PRA Health Sciences (ICON) in Blue Bell, PA. Maria currently works in study start-up and conduct for Oncology trials. Prior to joining PRA, Maria worked as a Clinical Research Coordinator at the Hospital of the University of Pennsylvania. As a CRC, Maria primarily worked on Multiple Sclerosis trials in the Department of Neurology. Maria was involved in all aspects of the clinical trials, including budget negotiations, regulatory and IRB submissions, and patient recruitment and study assessments. While at Penn, Maria earned the Rising Star of Clinical Research Excellence award. Maria completed her Bachelor of Science in Business Administration with a concentration in Marketing from Shippensburg University. Maria grew up in Philadelphia, PA and enjoys spending time with her family and friends.
NIKKI HIRSH, MS
Instructor
Senior Clinical Lead, IQVIA. In her earlier position at the Winship Cancer Institute at Emory University, Nikki successfully developed standard operating procedures, templates, and quality control forms. She has over 13 years of experience in clinical trials within private practice, corporate, and academic settings. Nikki has worked in the clinical research community in the areas of: CRC, CRA, regulatory, and management. She has a MS degree in Industrial and Organizational Psychology from Capella University.
LUCIA RODRIGUEZ, MS, ACRP-CP
Instructor
Lucia Rodriguez is currently the Research Director at EVOLVE Clinical Research. She is a bilingual clinical research professional and instructor with over a decade of experience managing all aspects of clinical trials at the site level; has assisted in the conduct of 200+ studies serving as the lead coordinator for the majority of those trials. Highly experienced in staff training/development and community outreach with an emphasis on minority recruitment initiatives. Experienced consultant providing creation of source documents, regulatory management, audit preparation services, quality control, and assurance in addition to site evaluation and analysis.
LAWRENCE MATARUTSE, MHA, CCRC
Instructor
Director, Clinical Research at University Medical Center New Orleans. Lawrence has also worked as a Clinical Research Manager at Children’s Healthcare of Atlanta, the largest pediatric hospital system in the Southeast. He holds a Master of Health Administration from Clayton State University. Lawrence started working in clinical research in 2003 as a Research Assistant and has worked in various roles at different institutions like the University of Zimbabwe and Emory University, and at hospitals including Grady Memorial Hospital and Children’s Healthcare of Atlanta. He brings in a wealth of research experience from managing drug and device trials in adult and pediatric research settings. Lawrence received his CCRC certification from ACRP in 2015.
LORI BANCTEL, MPH, CHRC
Instructor
Lori Banctel is currently the Director of Risk Based Quality Management and Analytics at Aperio Clinical Outcomes and was previously an Associate Director of Central Monitoring. Lori has a demonstrated history working in academic, hospital & health care industries. Exceptional skills in monitoring, auditing, research compliance, risk management, and leadership.
LATOYA HINTON-HOWERY, MPH
Instructor
Research Director, Next Innovative Clinical Research and Co-Founder, Noir Research Collective. LaToya Hinton-Howery, MPH is the CEO/Research Director of Next Innovative Clinical Research. She is a Medical Assistant by trade, holds a bachelor’s degree in Health Administration and a master’s in Public Health. LaToya has 10 years of pharmaceutical clinical research experience in various therapeutic areas including Women’s Health, Dermatology, Gastrointestinal, Cardiovascular, Respiratory, and Oncology. LaToya aspires to continue educating medical professionals on how to break into the world of clinical research.
LISA INCE, BS, CCRC, CCRA
Instructor
Current Project Manager, Previous Clinical Trial Manager at Syneos Health. In 2016, she was named the winner of the New Clinical Research Associate of the Year for the Americas by PharmaTimes. Mrs. Ince comes to Arizona from Chicago and has a Bachelor’s degree in Psychology from Elmhurst College. Mrs. Ince has 12 years of experience in and has held positions as, a Clinical Research Coordinator, Clinical Research Manager, and Clinical Research Associate. She was certified as a Clinical Research Coordinator 5 years ago and recently acquired her Certified Clinical Research Associate designation. Mrs. Ince is currently the Public Relations Coordinator for the Arizona Chapter of the ACRP and plans to start a Master’s program in Clinical Research this year. Mrs. Ince spends her free time with her two sons and husband and enjoys swing dancing.
KRISTIE DALY-BARNES, BS
Instructor
Associate Director, Illingworth Research Group. Previous Start-Up Team Manager, PPD. Kristie has been in the field of clinical research for over 18 years. She has worked on several pivotal diabetes studies such as Empa-REG, LEADER, and Devote Trials. She has also contracted with several pharmaceutical companies to assist with protocol development and feasibility studies from a site perspective as well as helping develop recruitment and retention initiatives. Outside of loving clinical research she is a workout junkie and a certified fitness instructor through AFAA and certified to teach 5 different Les Mills programs.
KENYETTA SIMS, M.A., CCRC
Instructor
Founder & CEO, Clinical Research Consulting, LLC. Previous Director of Clinical Research, Howard Brown Health. I am a self-motivated clinical research director/coordinator with management skills sets and education; I have an aptitude for managing people and projects without difficulty in multi-tasking and meeting deadlines.Specialties: Project Management, Training, Patient Care, Regulatory, GCP/ICH
KIKI DIORGU, M.D.
Instructor
Dr. Kiki Diorgu is a medical research professional with experience in both U.S and international clinical trials and regulatory affairs services. Dr. Diorgu currently serves as the Director of Clinical Operations for Morley Research Consortium, a full service CRO managing several multicenter and international clinical trials in the pharmaceutical and medical device industries. Dr. Diorgu has always had a passion for teaching. While in medical school, he was appointed as a teaching assistant to his peers in courses such as anatomy, physiology, cellular biology and biochemistry. He is the founder and lead instructor of a tutoring organization, Kikiprep, that provides educational services for medical students and medical graduates preparing to sit for the U.S medical boards (USMLE) as well as high school and college students preparing for tests such as the SAT, ACT and MCAT. Dr. Diorgu holds a Doctor of Medicine degree from Avalon University School of Medicine, currently lives in Atlanta, Georgia and enjoys playing soccer.
KINAL BHATT, MD, MPH
Instructor
Current Senior Director Product Leader, Lantheus. Previous Regional Medical Director – Medical Science Liaison. Experienced Clinical Research Professional with a demonstrated history of working on sponsor and investigator designed protocols in various therapeutic areas including Rheumatology, Neurology, Arthritis, Dermatology, Cardiovascular, Endocrinology, Quality Improvement. Driven By Results, Quality Assurance, Emotional Intelligence, Strong Communication Skills. Master’s degree focused in Public Health. Doctor of Medicine.
KIM KUNDERT, RN, BSN
Instructor
Current Senior Vice President Clinical Operations, Helios Clinical Research. Previous Senior VP of Site Development Services, Total Clinical Trial Management. Kim Kundert brings years of experience to Clinical Research Fastrack as an instructor. Kim was the former Senior Vice President of Operations at Synexus Research, the largest integrated clinical research network in the world. In this role, she was responsible for oversight of all operational activities at the site level. This included patient safety, enrollment on trials, and quality data. She worked closely with all departments to ensure standardization across the sites. This means following consistent SOPs, source templates, QA processes, and standardized regulatory binders. Kim currently works as the Senior VP of Site Development Services at Total Clinical Trial Management.
JULES FRISOLI, CP
Instructor
Principal Consultant, Phase 5 Clinical Research LLC. Jules is a dedicated, hardworking certified professional with 22 years of pharmaceutical industry experience with increasing responsibilities along his journey in clinical research. Oversight of monitoring has been his focal point for the last 8 years therefore, mentoring, managing, training, and remediating site personnel and CRAs is his expertise. Some of the areas Jules has worked in over the years include the following: TMF file auditing, FDA regulation, ICH GCP, CRO/Vendor management training, and more.
KASEY BOYNTON, BS
Instructor
Current Senior Director, Global Operations & Strategy Lead, Sanofi. Previous Director, Clinical Development at Syneos Health. Kasey Boynton brings over 12 years of combined experience in the development and implementation of global clinical programs within CROs, academia, and biotech companies. She has extensive experience in leading complex clinical protocols, cross-functional oversight and strategic execution that produces on-time results while fostering a highly-productive team environment. Kasey is a certified clinical research professional with extensive knowledge of ICH/GCP guidelines within the US, as well as governing authorities abroad. Kasey is based in Atlanta, GA and is an avid musician and fitness enthusiast.
JOHN CARLOS DIAZ, MS
Instructor
Clinical Research and Strategy Lead, Project Management, GeoSera LLC. John Carlos Diaz is the President and Owner of GeoSera Consulting, a Minority Business Enterprise that specializes in Clinical Research and Operations and executing Clinical Development Plans across multiple clinical trials. Prior to starting his own consulting company, John Carlos worked in Clinical Research for 10 years as a Clinical Operations Leader tasked with delivering endpoints within timelines and budgets. John Carlos has had various Clinical Operations roles with increasing levels of responsibility. Beginning at Merck in 2008, in Clinical Pharmacology through Cephalon/Teva managing phase I – IV, global, adult/pediatric clinical research from 2010 to 2015 and finally as the Clinical Operations leader for Braeburn Pharmaceuticals pipeline. Prior to entering the Clinical Research role, John Carlos was a Sr. Scientist at GSK within Drug Metabolism and Pharmacokinetics. After graduating from New York University in 2002 with a Bachelors in Biochemistry, John Carlos expanded his education base by obtaining professional certificates in Finance and Accounting from The Wharton School at the University of Pennsylvania, Clinical Research at Villanova University while finishing a Master’s degree in clinical research at George Washington University.
JENNIFER KOCOUR, MPH
Instructor
Chief Operating Officer at CCT Research. Jennifer Kocour is an instructor at Clinical Research Fastrack and has also served as Senior Director of Operations at Synexus Research, the largest integrated clinical research network in the world. She began as a Research Assistant, gained experience as a Study Coordinator, and later managed sites as a Regional Director. Currently, she is the Chief Operating Officer at CCT Research. She holds a Bachelor’s degree in Biology from Arizona State University and is a Certified Clinical Research Coordinator.
JEANNIE FARNSWORTH, MS, BS, CCRP, MRQA
Instructor
Current Associate Director Clinical Pharmacology, ICON. Previous Regional Clinical Scientist, ICON, and SOCRA National Board Member. Jeannie graduated with a Bachelor’s degree in Biology and Biochemistry with a minor in Business Administration from the University of Nevada-Reno. She earned her Master’s in Clinical Investigations from MGHIHP in association with Harvard Medical School. She has over 19 years of experience as a study coordinator, contractor, consultant, and monitor working on both drug and device clinical trials, predominantly assisting sites with study startup, protocol procurement, trial operations, and staff training. Her experience ranges from pediatric endocrinology and diabetes to ophthalmology and neurology. Her love and respect for this industry stemmed from her cherished relationships with study patients in all stages and phases of research. She is thrilled to teach at Clinical Research Fastrack to advance the field and process of Clinical Research.
HARVONYA PERKINS, BS
Instructor
Harvonya is a Clinical Research Site Manager at BFHC. She earned her BS in Biochemistry from Texas A&M University. She has worked in clinical research for over 7 years and strongly believes that increasing the competency of coordinators will increase research opportunities and outcomes for everyone involved in the industry.
JAMAICA CUNDIFF, BS
Instructor
In-house Clinical Research Associate II at Worldwide Clinical Trials. Jamaica is an Arizona native who obtained a B.S. in Care, Health, and Society with an emphasis in Social Work and Physiology from the University of Arizona. She has an extensive career history of working in behavioral health and hospice social work. Jamaica is also a Clinical Research Fastrack graduate who went on to conduct clinical research, specializing in Nephrology trials. At this stage, she was exposed to the vast structure of clinical research from study startup to closeout. The trials varied in complexity, primarily phase II-III, and included dialysis trials. Jamaica enjoys drawing, working out, spending time with her close friends, and taking her two dogs on adventures.
DENISE HAYES
Instructor
Denise Hayes serves as an instructor for Clinical Research Fastrack as well as a Senior Clinical Research Associate at PRA Health Sciences (ICON.) She was formerly the Site Manager in Dallas Texas at Synexus Research, the largest clinical research site network in the world. Denise joined Synexus (formerly Radiant Research) in 2011 as a Certified Clinical Research Coordinator. Her clinical research experience ranges from Phase 1 to Phase 4 clinical trials and is very diverse including indications such as HIV, Rheumatoid Arthritis, Neurology, Endocrinology, Women’s Health, Gastroenterology, Osteoarthritis, Osteoporosis, Dyslipidemia, and Vaccines to name a few.
ELIZABETH WEEKS-ROWE, LVN, CCRA
Instructor
Current Senior CRA, Merck. Previous Principal CRA at PPD, Author, Speaker. Elizabeth has 21 years of clinical research experience, including work as a study coordinator, CRA, CRA Trainer, and CRA manager. She has been an Association of Clinical Research Professionals (ACRP), Certified Clinical Research Associate (CCRA) since 2004. She is a frequent speaker at clinical research industry conferences as well as a requested speaker at both ACRP and SOCRA local chapter events. She has written numerous articles for clinical research publications, such as ACRP, CenterWatch, Pharmatimes, Clinical Leader, and the Journal of Best Research Practices. She also wrote the 2016 and 2018 updates to “The CRAs Guide to Monitoring Clinical Research” and the 2019 updates to “The PIs Guide to Conducting Clinical Research”, published by CenterWatch. She is a staff instructor for Clinical Research Fastrack and works as a Principal CRA in study start-up for Pharmaceutical Product Development (PPD), a global CRO.
GURPREET BRAR, MD MDA
Instructor
Current Clinician/ Director, Clinical Development and Operations, Pfizer. Previous Director Clinical Operations, Global Blood Therapeutics. Gurpreet has worked in clinical research for over 15 years, having managed global project teams, clinical teams, and has experience as a study coordinator, field CRA, Clinical Team Lead, Project Manager, and Director in Project Management. He excels at global team leadership, risk management, and training and development of both project teams and site staff. He has either worked in or led global teams in all regions of the world. Gurpreet has extensive oncology experience, both as a CRA and Project Manager, having worked in Phases I-III in both solid tumor and hematologic malignancies. His strengths include supporting the patient recruitment and retention efforts and to help advise study sites in these efforts, as well as assisting with managing any risks and training around the product reconstitution guidelines.Gurpreet is multi-lingual across four different languages and holds a Medical Degree from Russia. He is based in Phoenix, Arizona.
CHRISTINA CHONG, BSN
Instructor
Christina Chong currently works as the Principal, Clinical Data Reviewer at Biogen. She was previously the Clinical Data Manager at Loxo Oncology at Lilly. After obtaining a bachelor’s degree in Economics, she worked in the technology sector for a few years before deciding that healthcare – making a positive impact in peoples’ lives – was her true calling. Christina obtained a bachelor’s degree in Nursing from Arizona State University and entered the Clinical Research profession. She has worked as a coordinator in a variety of for-profit and non-profit organizations for over 5 years in various indications including nephrology, interventional nephrology, Phase I oncology, Alzheimer’s, Parkinson’s, and more. Christina is excited to share her enthusiasm and experiences in the clinical research profession blended with a financial and operational perspective. In her spare time, she enjoys hiking, cooking, tinkering at the piano, and playing board games with her kids.
DANIEL PÉREZ, BS, CCRP
Instructor
Current Director, Health Equity Strategy at Worldwide Clinical Trials. Previous President & CEO at MACRO Trials, Rebel Clinical Researcher. Leveraging skills acquired from over ten years of progressive clinical research experience, I help pharmaceutical and medical device companies accelerate successful therapeutic launches by optimizing clinical site performance, enabling sponsors’ access to real-world data to inform commercial success, and deploying inclusive multi-channel patient-centric participant recruitment/retention strategies that yield a diverse and representative patient population.
CHARLES WRIGHT
Instructor
Director, Merck. Charles Wright is a Senior Clinical Researcher with a career in clinical research lasting over 20 years. He managed the Patient Service Centers and technicians for over 40 sites for Labcorp. He subsequently moved over to Clinical Research Organizations monitoring, managing, and auditing clinical trials in the US and internationally. He partnered with pharmaceuticals companies to utilize his expertise in conducting clinical trials from Phase I through Phase IV adhering to ICH/GCP guidelines. Currently, he runs a private consulting firm providing project management, clinical monitoring, quality analysis and training for medical professionals and serves as a director at Merck.
AMY RAYMOND, PHD, PMP
Instructor
Current Executive Director Therapeutic Strategy Lead, Worldwide Clinical Trials. Previous Senior Director of Therapeutic Expertise, Center for Rare Diseases at ICON (formerly PRA Health Sciences). Amy was originally trained as a molecular biologist and has over 20 years of experience across all points of drug discovery and drug development. She has served as a field CRA on trials for neurodegenerative diseases such as ALS and Parkinson’s Disease. Amy enjoys continuing to grow as a clinical researcher, sharing her experiences, and helping expand the talent pool in the exciting and rewarding field of clinical research. As a graduate of the Clinical Research Fastrack program, she is thrilled to return as an instructor. She is a member of SoCRA, as well as a board member in her local chapter of ACRP. Amy and her husband returned to Phoenix after more than 20 years away, and could not be happier to be back in the Valley of the Sun!
AMBER S. ROBERTS, MBA
Instructor
Associate Director, Clinical Research – Oncology, Novartis Oncology. Amber has over 15 years of experience in a variety of roles including research compliance, quality, coordinator, and management roles in the areas of pharmacology, oncology, and neurology. She completed her bachelor’s at the University of Arizona in Tucson, AZ, her master’s at Temple University in Philadelphia, PA, and is currently pursuing her doctorate in Business Administration at Temple University. Prior to attending the University of Arizona, Amber grew up in Northern California and now calls Center City Philadelphia home. Amber enjoys visiting with friends and family, traveling, trying new restaurants, reading, and the performing arts.
WHY IT MATTERS TO US
The Silberman brothers’ mission for Clinical Research Fastrack is to improve the quality and progress of clinical research by educating and empowering research professionals with the skills they need to excel.
WHY IT MATTERS TO US
The Silberman brothers’ mission for Clinical Research Fastrack is to improve the quality and progress of clinical research by educating and empowering research professionals with the skills they need to excel.
