Job Description
Join Boston Medical Center's prestigious Clinical Research Division as a Clinical Research Coordinator and play a pivotal role in advancing medical breakthroughs. We seek a passionate professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. This opportunity offers unparalleled mentorship in cutting-edge oncology research with direct impact on patient care.
Boston Medical Center is a leading academic medical center renowned for its commitment to health equity and innovation. Our state-of-the-art facilities and collaborative environment provide the ideal setting for professional growth in clinical research.
Responsibilities
- Coordinate multi-site clinical trials from protocol development to closeout
- Ensure strict adherence to FDA regulations and ICH-GCP guidelines
- Recruit, screen, and enroll eligible study participants with cultural sensitivity
- Manage electronic data capture systems and maintain accurate regulatory documentation
- Train and monitor site staff on protocol procedures and compliance standards
- Prepare and submit regulatory submissions to IRB and sponsors
- Act as primary liaison between investigators, sponsors, and regulatory bodies
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) certification required
- Proficiency in electronic data capture systems (e.g., Medidata Rave)
- Exceptional organizational skills with attention to regulatory detail
- Strong interpersonal skills for effective patient and team communication
- Proven ability to manage competing priorities in a fast-paced environment
- Knowledge of HIPAA and 21 CFR Part 11 compliance requirements