Job Description
Join Boston Medical Center's pioneering research division where innovation meets compassionate care. As a Clinical Research Coordinator, you'll drive breakthroughs in cardiovascular medicine while working in a state-of-the-art facility. Our multidisciplinary team values collaboration, integrity, and scientific rigor. Enjoy competitive benefits, professional development opportunities, and the chance to transform patient lives through cutting-edge clinical trials.
Responsibilities
- Manage clinical trial protocols from initiation to closeout ensuring compliance with FDA regulations and GCP
- Coordinate investigator meetings, site monitoring visits, and regulatory submissions
- Oversee patient recruitment, enrollment, and retention strategies
- Maintain accurate electronic data capture systems and source documentation
- Adverse event reporting and safety monitoring per protocol requirements
- Train and supervise research staff on SOPs and regulatory guidelines
- Prepare regulatory documents, IRB submissions, and study reports
Qualifications
- Bachelor's degree in life sciences, nursing, or related clinical field
- Minimum 3 years clinical research coordination experience in cardiovascular trials
- Certification as a Clinical Research Professional (ACRP or SOCRA)
- Expertise in FDA regulations, ICH-GCP, and clinical trial management systems
- Strong proficiency in electronic data capture platforms (e.g., Medidata Rave)
- Exceptional organizational skills with attention to regulatory documentation
- Ability to manage multiple protocols simultaneously in a fast-paced environment