Job Description
Join Boston Medical Center's cutting-edge research division and help pioneer breakthroughs in patient care. We're seeking a meticulous Clinical Research Coordinator to manage pivotal clinical trials, ensuring regulatory compliance and data integrity. Collaborate with interdisciplinary teams including physicians, biostatisticians, and regulatory experts to advance medical innovations. Enjoy competitive benefits, professional development opportunities, and the chance to impact global healthcare standards.
Responsibilities
- Design, implement, and monitor clinical trial protocols in alignment with FDA/ICH guidelines
- Recruit, screen, and enroll study participants while maintaining ethical standards
- Collect, verify, and analyze clinical data using electronic data capture systems
- Prepare regulatory submissions (INDs, IRB protocols) and ensure audit readiness
- Coordinate with CROs, sponsors, and investigative sites for seamless trial execution
- Maintain accurate documentation in electronic trial master files (eTMF)
Qualifications
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Minimum 3 years of clinical trial coordination experience in therapeutic areas
- Proficiency in EDC systems (e.g., Medidata Rave, Oracle Inform)
- Deep understanding of GCP, FDA regulations, and 21 CFR Part 11
- Exceptional organizational skills with attention to detail and documentation accuracy
- Strong interpersonal skills for stakeholder collaboration and patient engagement