Job Description
Join Boston Medical Center's prestigious clinical research division and shape the future of healthcare innovation. We seek a meticulous Clinical Research Coordinator to manage complex oncology trials while ensuring regulatory compliance and patient safety. This pivotal role bridges cutting-edge science with compassionate patient care in an academic medical environment.
Our state-of-the-art research facility collaborates with industry leaders and NIH-funded studies, offering unparalleled opportunities for professional growth. Enjoy comprehensive benefits including tuition reimbursement, flexible scheduling, and dedicated mentorship from board-certified physicians.
Responsibilities
- Oversee all aspects of oncology clinical trials including protocol implementation, patient recruitment, and data management
- Ensure strict adherence to FDA regulations, GCP standards, and institutional IRB protocols
- Coordinate multi-disciplinary research teams including physicians, nurses, and biostatisticians
- Maintain accurate electronic lab records (REDCap) and regulatory documentation
- Conduct comprehensive patient education and informed consent procedures
- Monitor adverse events and safety reporting per FDA guidelines
- Analyze trial data and prepare comprehensive regulatory submissions
Qualifications
- Master's degree in Clinical Research, Public Health, or related field
- 3+ years experience coordinating oncology clinical trials
- Certified Clinical Research Professional (CCRP) certification required
- Proficiency in electronic data capture systems (REDCap, Medidata Rave)
- Demonstrated knowledge of FDA 21 CFR Part 11 compliance
- Exceptional attention to detail and documentation accuracy
- Strong interpersonal skills for patient interactions and team coordination
- Experience with IRB submissions and regulatory audits