Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and become a vital part of groundbreaking medical advancements. We seek a detail-oriented professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. Collaborate with multidisciplinary teams including physicians, nurses, and biostatisticians in our state-of-the-art facilities.
BMC offers comprehensive benefits including health insurance, retirement plans, and continuing education stipends. This hybrid role (3 days remote/2 days onsite) provides exceptional work-life balance while contributing to life-changing research.
Responsibilities
- Design and execute clinical trial protocols in compliance with FDA and ICH-GCP standards
- Recruit, screen, and enroll eligible study participants while maintaining ethical standards
- Manage comprehensive electronic data capture systems and ensure data integrity
- Coordinate with IRB for protocol amendments and adverse event reporting
- Train clinical staff on trial procedures and regulatory requirements
- Monitor trial progress through regular site visits and audit preparation
- Prepare regulatory submissions and maintain study documentation
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience
- Certified Clinical Research Professional (CCRP) certification required
- Proficiency in electronic data capture systems (e.g., Medidata Rave)
- Strong knowledge of FDA regulations and ICH-GCP guidelines
- Exceptional attention to detail and documentation skills
- Excellent interpersonal and communication abilities
- Experience with oncology trials highly desirable