Job Description
Join Boston Medical Innovations, a leader in cutting-edge clinical trials, as we revolutionize patient care through groundbreaking research. We're seeking a meticulous Clinical Research Coordinator to drive our oncology studies forward. In this pivotal role, you'll manage complex protocols, ensure regulatory compliance, and collaborate with multidisciplinary teams to accelerate therapeutic innovations. Our state-of-the-art facility in Boston's Longwood Medical Area offers unparalleled resources and a culture of scientific excellence.
Why Choose Us?
- Access to 12 specialized research centers
- Collaborative environment with MIT and Harvard partnerships
- Comprehensive benefits including tuition reimbursement
- Industry-leading professional development programs
Responsibilities
- Oversee end-to-end management of Phase II/III oncology clinical trials
- Ensure strict adherence to FDA regulations, ICH-GCP, and institutional protocols
- Coordinate patient recruitment, screening, and retention strategies
- Manage electronic data capture systems and maintain accurate study documentation
- Liaise with IRB, sponsors, and regulatory authorities for protocol amendments
- Mentor junior staff and conduct site audits for compliance
- Analyze trial data and prepare comprehensive regulatory submissions
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 3+ years of oncology clinical trial coordination experience
- Certified Clinical Research Professional (CCRP) certification
- Proficiency in Medidata Rave and CTMS systems
- Demonstrated knowledge of 21 CFR Part 11 and HIPAA compliance
- Exceptional organizational skills with attention to regulatory detail
- Strong written/verbal communication for stakeholder interactions
- Experience managing complex multi-site trials preferred