Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and contribute to groundbreaking medical breakthroughs. We're seeking a passionate professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. This role offers the opportunity to work with world-class physicians in a cutting-edge academic medical environment.
BMC is an Equal Opportunity Employer committed to diversity and inclusion. We offer competitive benefits, professional development opportunities, and a collaborative culture that values innovation in healthcare research.
Responsibilities
- Oversee end-to-end clinical trial execution including protocol development, site management, and regulatory submissions
- Recruit, screen, and enroll study participants while maintaining ethical standards and informed consent protocols
- Manage electronic data capture systems, ensure data integrity, and generate comprehensive study reports
- Coordinate with multidisciplinary teams including physicians, nurses, and biostatisticians
- Monitor adverse events and ensure compliance with FDA regulations and GCP guidelines
- Maintain accurate documentation for audits and inspections
Qualifications
- Bachelor's degree in life sciences, nursing, or related healthcare field (Master's preferred)
- Minimum 3 years of clinical research coordination experience in an academic medical center
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave, REDCap)
- Deep knowledge of FDA regulations, ICH-GCP, and IRB procedures
- Exceptional organizational skills with ability to manage multiple concurrent trials
- Strong written communication skills for preparing study protocols and regulatory documents