Job Description
Join our pioneering team at Boston Medical Research Institute, where innovation meets compassionate care. We're seeking a Senior Clinical Research Coordinator to lead groundbreaking studies in oncology. As a key member of our dynamic research department, you'll contribute to life-changing medical advancements while collaborating with world-class physicians and scientists. Our state-of-the-art facilities offer cutting-edge resources, and we're committed to your professional growth through continuous training and mentorship. If you're passionate about accelerating medical breakthroughs and improving patient outcomes, this is your opportunity to make a lasting impact.
Responsibilities
- Oversee end-to-end clinical trial execution, ensuring protocol adherence and regulatory compliance (FDA, GCP, ICH guidelines)
- Manage patient recruitment, enrollment, and retention strategies for oncology studies
- Coordinate cross-functional teams including principal investigators, biostatisticians, and data managers
- Maintain meticulous documentation of adverse events, efficacy data, and study milestones
- Lead site initiation visits, routine monitoring, and study closeout procedures
- Develop and maintain robust relationships with healthcare partners and research subjects
- Analyze study data and contribute to regulatory submissions and publication materials
Qualifications
- Master's degree in life sciences, nursing, or related field; PhD preferred
- 5+ years of clinical research coordination experience in oncology or therapeutic areas
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Expertise in EDC systems (Medidata Rave, Oracle InForm) and CTMS platforms
- Proven track record of managing complex multi-center trials with 50+ subjects
- Deep knowledge of FDA 21 CFR Part 312 and ICH-GCP regulations
- Exceptional problem-solving skills with ability to troubleshoot protocol deviations
- Strong leadership experience with cross-functional teams and external partners