Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and drive groundbreaking advancements in patient care. We're seeking a meticulous professional to oversee clinical trials across our oncology and cardiology departments. Enjoy competitive benefits, cutting-edge resources, and opportunities to publish in leading medical journals. Your work will directly impact patient outcomes while collaborating with world-renowned physicians.
Responsibilities
- Manage end-to-end clinical trial execution including protocol development, site initiation, and regulatory compliance
- Coordinate patient recruitment, informed consent processes, and data collection per FDA guidelines
- Maintain accurate electronic lab records and ensure data integrity through source documentation
- Liaise with sponsors, IRB, and multidisciplinary teams to resolve protocol deviations
- Prepare regulatory submissions and ensure ongoing compliance with GCP standards
- Monitor adverse events and implement corrective action plans
- Train clinical staff on trial protocols and study procedures
Qualifications
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience with FDA-regulated trials
- Certified Clinical Research Professional (CCRP) or ACRP certification required
- Proficiency in electronic data capture systems (e.g., Medidata Rave, REDCap)
- Demonstrated knowledge of ICH-GCP and 21 CFR regulations
- Exceptional attention to detail and documentation skills
- Strong organizational abilities with capacity to manage multiple protocols
- Excellent interpersonal communication for patient and stakeholder interactions