The RAPS NC Local Networking Group is pleased to present a panel discussion bringing together industry leaders and academic faculty to examine the current landscape of clinical research and regulatory affairs education in North Carolina and beyond. Panelists will share perspectives on the academic curricula that best prepare students and early-career professionals for meaningful, sustainable careers in clinical research and regulatory affairs. The conversation will explore where current programs excel, where critical gaps remain, and what new curricular offerings the profession needs to develop in response to an evolving regulatory and research environment. Panelists will also address professional development and training priorities for faculty and clinical research staff who are committed to advancing program quality and workforce readiness. This event is designed for clinical research professionals, regulatory affairs practitioners, academic faculty, students, and anyone with an interest in shaping the educational infrastructure that supports these fields. Attendees can expect candid dialogue, actionable insights, and an opportunity to connect with educators and industry leaders who are actively invested in growing the profession.
The RAPS NC Local Networking Group is pleased to present a panel discussion bringing together industry leaders and academic faculty to examine the current landscape of clinical research and regulatory affairs education and workforce in North Carolina and beyond. Panelists representing the Association of Clinical Research Professionals (ACRP), Black Women in Clinical Research (BWICR), Durham Technical Community College, North Carolina Central University Biomanufacturing Research Institute and Technology Enterprise (BRITE), Northeastern University College of Professional Studies, Duke University School of Medicine, and the University of North Carolina at Chapel Hill Eshelman School of Pharmacy will share perspectives on the academic curricula that best prepare students and early-career professionals for meaningful, sustainable careers in clinical research and regulatory affairs. The conversation will explore where current programs excel, where critical gaps remain, and what new curricular offerings the profession needs to develop in response to an evolving regulatory and research environment. Panelists will also address professional development and training priorities for faculty and clinical research staff who are committed to advancing program quality and workforce readiness. This event is designed for clinical research professionals, regulatory affairs practitioners, academic faculty, students, and anyone with an interest in shaping the educational infrastructure that supports these fields. Attendees can expect candid dialogue, actionable insights, and an opportunity to connect with educators and industry leaders who are actively invested in growing the profession.
North Carolina Central University
1801 Fayetteville St
Durham, NC 27707
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation. All cancellation requests must be submitted in writing to [email protected]. Cancellations will receive a full refund minus a 20% administrative fee.RAPS is unable to accept cancellations by phone.
Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email [email protected]with the event title, name of the original registrant and the contact information for the new attendee.
A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.
Contact the RAPS Support Center:
Call +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email [email protected].

Senior Manager, Regulatory Affairs , RAPS NC Chair BD, Moderator

Vice President, Regulatory Affairs and Quality Assurance, Mycovia Pharmaceuticals



Associate Dean, Executive Director, Regulatory Affairs and Quality, Office of Regulatory Affairs and Quality (ORAQ) , Duke University School of Medicine

Research Assistant Professor, Program Lead, North Carolina Central University

Clinical Quality Assurance Specialist , BWICR Ambassador Ora Inc.


Program Director and Associate Professor, UNC Eshelman School of Pharmacy

Senior Manager, Regulatory Affairs , RAPS NC Chair BD, Moderator
Sequita Lindsey is the Senior Manager of Regulatory Affairs Infection Prevention US, Surgery at BD (Becton, Dickinson and Company), bringing more than 19 years of experience across the medical device, pharmaceutical, and combination product sectors. Her career began on the manufacturing floor and grew through the ranks of regulatory affairs, giving her a hands-on understanding of every stage of the product lifecycle and a deep, unwavering commitment to patient safety.
In addition to her role at BD, Sequita serves as an Adjunct Assistant Professor at the University of North Carolina at Chapel Hill Eshelman School of Pharmacy and Adjunct Professor at North Carolina Central University, Biomanufacturing Research Institute Technology Enterprise (BRITE), reflecting her passion for developing the next generation of regulatory professionals.
Sequita holds a Master of Science in Regulatory Affairs (MSRA) from Northeastern University and a Bachelor of Science from Winston-Salem State University. She holds the Regulatory Affairs Certification (RAC) in Global Scope and is a Fellow of the Regulatory Affairs Professionals Society (FRAPS), one of the highest distinctions RAPS confers on its members.
As Chair and President of the newly formed RAPS North Carolina Local Networking Group, Sequita is committed to building a connected, inclusive community for regulatory, quality, and compliance professionals across the state.

Vice President, Regulatory Affairs and Quality Assurance, Mycovia Pharmaceuticals
Jocelyn Jennings, MSRA, RAC-US, RAC-Drugs, RAPS-Devices, FRAPS is Vice President, Regulatory Affairs and Quality Assurance at Mycovia Pharmaceuticals, Inc. Ms. Jennings has over 25 years of extensive global regulatory affairs, quality assurance, pharmacovigilance, and global clinical trial experience in drugs, biologics, medical devices and combination products. Ms. Jennings began her career in analytical and hospital laboratories analyzing industrial samples, toxicology and clinical chemistry samples and performing specialty tests. She has had leadership roles at small and large biopharmaceutical and medical device companies in various therapeutic areas such as oncology, immunology, women’s health, and rare diseases. Ms. Jennings is an adjunct professor in Northeastern University’s College of Professional Studies in the Masters of Regulatory Affairs Program. Ms. Jennings is a member of the Drug Information Association, Society of Quality Assurance, North Carolina Chapter Society of Quality Assurance, and Regulatory Affairs Professional Society (RAPS). She is actively involved as a volunteer with RAPS as Lead Editor and Author of RAPS books. Ms. Jennings also serves on the RAPS Editorial Advisory Committee, is a Regulatory Affairs Certification Board Member, RAPS Global Board of Director and is a RAPS Fellow. Ms. Jennings obtained her MS in regulatory affairs from Northeastern University.
:
https://www.linkedin.com/in/jocelyn-jennings-ms-rac-us-rac-drugs-rac-devices-fraps-66736b4/

Program Director, Clinical Research Program
Dr. Sharleen Traynor is the Director of the Clinical Research program at Durham Technical Community College. In this role, she oversees the education and training of students pursuing careers in clinical research, ensuring they are provided with a curriculum that meets the professional standards of the research community. An epidemiologist by training, Dr. Traynor has over 20 years of public health and clinical research experience working in roles ranging from CRC, data analyst, and clinical project manager. She now focuses on workforce development efforts to advance the education of clinical research professionals. In addition to her responsibilities in higher education, Dr. Traynor serves on the Diversity Advisory Council for the Association of Clinical Research Professionals (ACRP) where she supports initiatives that increase representation across the clinical research workforce. She is also a member of the Community Partnered Research Network (CPRN) Executive Leadership Committee and the Executive Operations Committee for the Duke Clinical and Translational Sciences Institute
Associate Dean, Executive Director, Regulatory Affairs and Quality, Office of Regulatory Affairs and Quality (ORAQ) , Duke University School of Medicine
No bio provided

Research Assistant Professor, Program Lead, North Carolina Central University
No bio provided

Clinical Quality Assurance Specialist , BWICR Ambassador Ora Inc.
Rijhanique is a Clinical Quality Assurance Specialist with a Bachelor's degree in Biology and over 8 years of experience in the pharmaceutical industry, along with 5 years in clinical research. Her career spans laboratory quality, clinical trial operations, and regulatory compliance, where she has supported FDA audits and contributed to pre-approval testing for critical therapies, including HIV and asthma medications. She began her clinical research career as a Clinical Trial Assistant and advanced into a co-monitoring role, ensuring protocol and regulatory compliance at the site level. In her current role, Rijhanique leads internal, vendor, and site audits, working to ensure that clinical trials meet regulatory standards while prioritizing patient safety and data integrity. She also plays a key role in CAPA investigations, continuous improvement initiatives, and SOP development. Rijhanique is passionate about bridging the gap between education and industry and is committed to helping students and early-career professionals navigate and succeed in the clinical research and regulatory field.
Senior Research Associate , BWICR Ambassador Syneos Health
Jazmin Barnes is a Sr. Clinical Research Associate, content creator, and advocate dedicated to advancing diversity and excellence in clinical research. With over five years of experience in clinical trial operations, she specializes in quality control, audit readiness, database locking, and ensuring compliance with ICH-GCP standards across multi-site studies. Her work plays a critical role in bringing safe and effective treatments to patients while upholding the highest standards of data integrity.
Jazmin began her career in behavioral health after earning her degree in Psychology from North Carolina A&T State University before transitioning into clinical research. She is passionate about increasing representation in clinical trials and actively contributes to this mission as the Brand Ambassador Leader for Black Women in Clinical Research®.
Beyond her professional work, Jazmin leverages her platform as a content creator to educate, inspire, and mentor aspiring clinical research professionals. She shares insights on breaking into the industry, career growth, and mental health—empowering others to navigate their journeys with confidence and purpose.

Program Director and Associate Professor, UNC Eshelman School of Pharmacy
Patricia Termini, M.S., RAC, is the Director of the Master of Professional Science (M.P.S.) in Regulatory Science and an Associate Professor in the Division of Pharmacotherapy and Experimental Therapeutics. She has more than 25 years of experience in the pharmaceutical, biotechnology, and consulting industries focused on regulatory affairs strategy, execution, and project management. Ms. Termini has experience working cross-functionally on pre-approval and post-approval regulatory activities and has worked in multiple therapeutics areas including dermatology, infectious disease, oncology, and rare diseases. She has a M.S. degree in Regulatory Affairs and Quality Assurance from Temple University, is RAC certified, and has certificates in drug development and project managementWe have completed our migration to a new platform and are pleased to introduce the updated site.
What to expect: If you have an existing login, please RESET YOUR PASSWORD before signing in. After you log in for the first time, you will be prompted to confirm your profile preferences, which will be used to personalize content.
We encourage you to explore the new website and visit your updated My RAPS page. If you need assistance, please review our FAQ page.
We welcome your feedback. Please let us know how we can continue to improve your experience.