Job Description
Join our pioneering team at Boston Medical Research Institute, where innovation meets compassionate care. We're seeking a dynamic Senior Clinical Research Coordinator to lead groundbreaking studies in oncology and immunotherapy. As a key player in our clinical trials division, you'll shape the future of patient treatment protocols while working alongside world-renowned physicians and scientists. This role offers unparalleled opportunities for professional growth in a state-of-the-art facility with cutting-edge technology.
Our institute provides comprehensive benefits including competitive compensation, flexible scheduling, tuition reimbursement, and a robust wellness program. Enjoy a collaborative environment where your expertise directly impacts patient outcomes and medical breakthroughs.
Responsibilities
- Design and execute comprehensive clinical trial protocols ensuring regulatory compliance (FDA, ICH-GCP)
- Manage patient recruitment, enrollment, and retention strategies for diverse populations
- Oversee data collection, verification, and statistical analysis using REDCap and EDC systems
- Coordinate multi-disciplinary research teams including physicians, nurses, and biostatisticians
- Prepare and submit regulatory documentation to IRB and sponsor organizations
- Monitor adverse events and ensure protocol adherence through regular site visits
- Maintain accurate study documentation in compliance with 21 CFR Part 11
Qualifications
- Master's degree in Clinical Research, Nursing, or related health science field
- 5+ years of clinical trial coordination experience in oncology or immunology
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in FDA regulations, ICH-GCP, and clinical trial management systems
- Proven success in managing multi-center trials with complex protocols
- Exceptional data management skills with statistical software proficiency
- Strong leadership abilities with cross-functional team management experience
- Excellent written communication for regulatory submissions and study reports