Job Description
Join Boston Medical Center's cutting-edge research division as a Clinical Research Coordinator. You'll play a pivotal role in advancing medical breakthroughs while ensuring regulatory compliance and patient safety. This position offers the opportunity to work with leading physicians in a collaborative, mission-driven environment. We offer competitive benefits, professional development opportunities, and the chance to make a tangible impact on patient care.
Responsibilities
- Oversee clinical trial protocols from initiation to closure, ensuring adherence to FDA and GCP standards
- Recruit, screen, and enroll qualified study participants while maintaining ethical practices
- Manage trial documentation, including IRB submissions, consent forms, and regulatory filings
- Coordinate site monitoring visits and maintain accurate electronic data capture systems
- Analyze study data and prepare comprehensive reports for sponsor review
- Train clinical staff on study protocols and regulatory requirements
- Collaborate with multidisciplinary teams to troubleshoot protocol deviations
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) certification required
- Expertise in FDA regulations, ICH-GCP guidelines, and 21 CFR compliance
- Proficiency with electronic data capture systems (e.g., Medidata Rave)
- Exceptional organizational skills with attention to detail
- Strong written and verbal communication abilities
- Experience managing complex multi-site protocols