Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and shape the future of healthcare innovation. We're seeking a meticulous professional to orchestrate groundbreaking clinical trials while ensuring regulatory compliance and patient safety. In this impactful role, you'll collaborate with world-class physicians, manage complex study protocols, and contribute to life-changing medical breakthroughs.
BMC offers unparalleled career development, competitive benefits, and a mission-driven environment where your expertise directly impacts patient outcomes. If you're passionate about precision, ethical research, and transforming healthcare, apply today.
Responsibilities
- Coordinate multi-phase clinical trials from protocol development to final closeout
- Ensure strict adherence to FDA regulations, GCP standards, and IRB protocols
- Recruit, screen, and enroll qualified study participants while maintaining ethical standards
- Manage electronic data capture systems and maintain accurate regulatory documentation
- Monitor patient safety, adverse events, and protocol deviations
- Liaise between investigators, sponsors, and regulatory agencies
- Train staff on study procedures and regulatory compliance
- Prepare complex regulatory submissions and study reports
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience with therapeutic trials
- Certified Clinical Research Coordinator (CCRC) or ACRP certification
- Expertise in FDA regulations, ICH-GCP, and 21 CFR Part 820
- Proficiency in EDC systems (e.g., Medidata Rave, Veeva Vault)
- Exceptional attention to detail and documentation skills
- Strong interpersonal abilities for stakeholder collaboration
- Experience with oncology or cardiovascular trials preferred