Job Description
Join our prestigious research team at Boston Medical Center, where innovation meets compassionate care. We're seeking a Clinical Research Coordinator to drive groundbreaking studies that transform patient outcomes. In this pivotal role, you'll collaborate with leading physicians, manage complex protocols, and ensure regulatory compliance while advancing medical science.
Our state-of-the-art research facilities and multidisciplinary environment offer unparalleled opportunities for professional growth. Enjoy comprehensive benefits, flexible scheduling, and a commitment to work-life balance that's rare in healthcare research.
Responsibilities
- Design, implement, and oversee clinical trial protocols ensuring FDA and GCP compliance
- Recruit, screen, and enroll study participants while maintaining ethical standards
- Manage comprehensive data collection, analysis, and reporting using REDCap systems
- Coordinate with IRB, sponsors, and regulatory bodies for protocol approvals and amendments
- Train clinical staff on study procedures and maintain regulatory documentation
- Monitor adverse events and ensure timely safety reporting to regulatory authorities
- Present findings at conferences and contribute to peer-reviewed publications
Qualifications
- Master's degree in life sciences, nursing, or related field (BS with 3+ years experience considered)
- Certified Clinical Research Professional (CCRP) or equivalent certification preferred
- Minimum 3 years coordinating clinical trials in therapeutic area (oncology/neurology preferred)
- Expertise in regulatory compliance (FDA, ICH-GCP, HIPAA)
- Advanced proficiency in clinical trial management software (e.g., Oracle Clinical, Veeva)
- Strong data management skills with experience in EDC systems
- Exceptional communication skills for stakeholder engagement and patient education