Megan Roberts, M.S., CCRC, is a clinical research compliance specialist with the UF Health Cancer Institute’s Clinical Research Office.
Q: What is your hometown?
A: Edgewater, Florida.
Q: Describe your educational and professional background.
A: I have a bachelor’s degree in applied physiology and kinesiology and a master’s degree in clinical exercise physiology, both from the University of Florida. I spent my first 12 years in the field as a research coordinator and later an operations manager, working on a variety of successful aging and mobility studies. I eventually transitioned into my current path as a compliance specialist at the Cancer Institute.
Q: How did you get into your current career path and how many years have you been in the role?
A: I have been in my current role for about 3 1/2 years. I have always been passionate about research and the impact it can have on patients’ lives; moving into compliance felt like a natural evolution of my research career.
Q: What is a typical day like in your job?
A: I spend much of my time reviewing research charts to ensure adherence to study protocols, regulatory requirements and department policies. I also work closely with teams to address findings and resolve queries, ensuring that documentation is in place and accurately reflects the high standards of our institute.
Q: What is the most rewarding part of working for the UF Health Cancer Institute?
A: The most rewarding aspect is knowing that my work supports research that has the potential to change and even save lives. I also enjoy collaborating with and supporting our hard-working study teams.
Q: How do you keep your skills current and continue to learn and grow?
A: I attend continued education lectures, seminars and workshops and have maintained my Certified Clinical Research Coordinator (CCRC) certification for over 10 years through the Association of Clinical Research Professionals (ACRP). My daily work is also a continued learning experience; each trial and review has its own unique set of circumstances to work through while maintaining compliance with research regulations and guidelines.
Q: Describe how you would spend your ideal day off from work.
A: My ideal day off would be spent at a new ballpark watching the Yankees play or at home curled up with a good book.
Q: What advice would you give someone interested in pursuing a career in research compliance?
A: As a compliance specialist, it is important to approach compliance reviews as a partnership to build trust with your study teams. It’s also important to embrace the “why” behind the rules. Although we will always ask for documentation, compliance isn’t just about checklists and paperwork; it’s about protecting the participants and ensuring the validity of research.
