Regulatory Science Symposium: “Keys to a Clinical Trial: Management and Operations” Session 8 - Peer to Peer Panel: Real-World Opportunities and Challenges in Clinical Trial Project Management (2024)

Regulatory & Quality Sciences
Study & Site Management
Apurva Uniyal, MA, MS

Regulatory Innovation Research Scientist

Karen Manrique, MS

Project Administrator, Regulatory Knowledge Support

Denise De Los Santos, BA

Patient Recruitment and Navigation Specialist

Competencies: Patient Recruitment, Patient Enrollment, Project Management, Regulatory Science, Education, Policy and Procedures, Institutional Review Board (IRB), Community Engagement, Clinical Research Coordinators (CRCs), Budget

Course Syllabus/Topics:

  1. Introductions
    1. Apurva Uniyal, Regulatory Innovations Research Scientist at the D.K. Kim International Center for Regulatory Science, which is housed within the USC Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences, Department of Regulatory and Quality Sciences
    2. Karen Manrique, Project Administrator at the Southern California Clinical and Translational Science Institute, Regulatory Knowledge and Support core
    3. Denise De Los Santos, Patient Recruitment and Navigation Specialist at the Southern California Clinical and Translational Science Institute, Clinical Research Support core.
  1. Questions and Answers
    1. Panelists draw upon their experiences to respond to questions regarding real-world opportunities, challenges, and potential solutions in the management of clinical trials.
  2. Thank you!

Acknowledgements:
Accompanying text created by:
Roxy Terteryan, Project Administrator, SC CTSI (atertery@usc.edu)
Rushaanaaz Sokeechand, Student Worker

NIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.