Job Description
Join our pioneering team at Boston Biomedical Research Institute, where we're revolutionizing patient care through groundbreaking clinical trials. As a Clinical Research Coordinator, you'll be at the forefront of medical innovation, ensuring the integrity of our oncology studies while directly impacting treatment outcomes. We offer a collaborative environment with cutting-edge facilities and opportunities for professional growth in one of America's premier healthcare hubs.
Responsibilities
- Oversee clinical trial protocols from initiation to completion, ensuring FDA and GCP compliance
- Manage participant recruitment, screening, and retention strategies for oncology studies
- Coordinate multi-disciplinary research teams including physicians, nurses, and data specialists
- Maintain accurate electronic Case Report Forms (eCRFs) and regulatory documentation
- Analyze and interpret clinical data to prepare interim reports for sponsors
- Train site staff on protocol amendments and regulatory updates
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in oncology trials
- Certified Clinical Research Professional (CCRP) certification required
- Proficiency in electronic data capture systems (e.g., Medidata Rave)
- Demonstrated knowledge of ICH-GCP and FDA regulations
- Exceptional organizational skills with attention to detail
- Strong written and verbal communication abilities