Job Description
Join Boston Medical Center's prestigious clinical research team as a Clinical Research Coordinator and drive groundbreaking medical innovations. We're seeking a meticulous professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. With access to cutting-edge facilities and interdisciplinary collaboration, you'll contribute to life-changing treatments while advancing your career in a supportive academic environment. BMC offers competitive benefits, professional development stipends, and opportunities for publication in leading medical journals.
Responsibilities
- Design, implement, and monitor clinical trial protocols in accordance with FDA and GCP guidelines
- Recruit, screen, and enroll eligible participants while maintaining strict confidentiality standards
- Manage study budgets, vendor contracts, and regulatory documentation (IRB submissions, adverse event reporting)
- Coordinate multidisciplinary teams including physicians, nurses, and biostatisticians
- Ensure data integrity through electronic data capture (EDC) systems and source verification
- Prepare comprehensive study reports for sponsors and institutional review boards
Qualifications
- Bachelor's degree in life sciences, nursing, or related field; Master's preferred
- 2+ years clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) or ACRP certification
- Proficiency in REDCap, Medidata Rave, or similar EDC platforms
- Deep knowledge of ICH-GCP, FDA regulations, and 21 CFR compliance
- Exceptional organizational skills with ability to manage multiple concurrent protocols
- Strong written/verbal communication for patient education and team coordination