Job Description
Join Boston Medical Center's cutting-edge research division as a Clinical Research Coordinator and contribute to groundbreaking medical advancements. We seek a meticulous professional to ensure regulatory compliance, patient safety, and protocol adherence across multi-center clinical trials. This pivotal role bridges scientific innovation and patient care in one of America's premier academic medical centers.
Responsibilities
- Oversee daily clinical trial operations including patient recruitment, informed consent, and protocol compliance
- Maintain accurate regulatory documentation (FDA, IRB, ICH-GCP) and ensure audit readiness
- Coordinate interdisciplinary teams (physicians, nurses, lab technicians) and manage trial budgets
- Monitor adverse events and ensure timely reporting to regulatory authorities
- Analyze trial data and prepare comprehensive reports for sponsors and ethics committees
- Train clinical staff on trial protocols and regulatory requirements
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Minimum 3 years clinical trial coordination experience in oncology or cardiology
- Expertise in electronic data capture systems (e.g., Medidata Rave, Oracle Clinical)
- Demonstrated knowledge of FDA 21 CFR Part 812 and ICH-GCP guidelines
- Exceptional organizational skills with attention to regulatory detail
- Strong written/verbal communication and conflict resolution abilities