The Clinical Research Coordinator Development Program (CRCDP) provides flexible, self-paced online learning and hands-on training for both working professionals and full-time students, with completion possible in as little as 3 months.
Through this opportunity, you will have the chance to:
- Build a rewarding career contributing to scientific advancements.
- Collaborate closely with physicians and nurses to ensure the well-being of study participants.
- Collect and manage accurate data to maintain detailed records.
- Implement research protocols and understand participant eligibility.
The training includes:
Self-Paced Learning
Regulatory Guidelines
Ethics
Human Subject Protection
Study Coordination
Experiential Learning
Competency checkpoints
Practical application of skills
Mentorship
Continued Professional Development
Seminars and Workshops
Peer Networks
Access to library of training materials
Applicant Qualifications
- Successful candidates may have clinical degrees but are not limited to those with clinical experience.
- All candidates should have a desire to engage in research. Minimum education requirement of an associate degree, or at least 5 years of relevant work experience.
Contact:
E-mail: iscore-rc.rcm@upr.edu
Phone: 787-758-2525, Ext. 2173
