Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and drive breakthroughs in patient care. We're seeking a detail-oriented professional to manage complex clinical trials while ensuring regulatory compliance and data integrity. Work alongside world-renowned physicians in our state-of-the-art facilities, contributing to life-changing medical advancements. This hybrid role offers competitive benefits, professional development opportunities, and the chance to make a tangible impact in healthcare innovation.
Responsibilities
- Oversee all aspects of clinical trial protocols including patient recruitment, informed consent, and data collection
- Ensure strict adherence to FDA regulations, GCP guidelines, and institutional policies
- Coordinate interdisciplinary teams including physicians, nurses, and lab technicians
- Manage electronic data capture systems and maintain accurate trial documentation
- Monitor adverse events and prepare regulatory submissions for IRB approval
- Analyze trial data and prepare comprehensive reports for sponsors and internal stakeholders
- Train clinical staff on protocol procedures and regulatory requirements
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in hospital or academic setting
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in FDA regulations, ICH-GCP, and 21 CFR compliance
- Proficiency in electronic data capture systems (e.g., Medidata Rave, REDCap)
- Exceptional organizational skills with ability to manage multiple concurrent trials
- Strong written communication skills for regulatory documentation and reporting
- Experience with oncology or cardiology trials preferred