Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and drive groundbreaking advancements in healthcare innovation. We're seeking a meticulous professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. This role offers unparalleled opportunities to collaborate with world-class physicians and contribute to life-changing medical discoveries. Our state-of-the-art facilities and supportive research environment provide the ideal platform for professional growth.
Responsibilities
- Oversee all aspects of clinical trials including protocol development, site management, and regulatory submissions
- Coordinate IRB approvals, informed consent processes, and HIPAA compliance
- Manage data collection, CRF design, and electronic data capture systems
- Liaise with sponsors, investigators, and regulatory agencies
- Train clinical staff on trial protocols and GCP standards
- Monitor trial progress, resolve protocol deviations, and ensure audit readiness
- Prepare comprehensive study reports and regulatory documentation
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience with FDA/ICH-GCP compliance
- Certified Clinical Research Professional (CCRP) certification required
- Expertise in electronic data capture systems (e.g., Medidata Rave, REDCap)
- Strong knowledge of FDA regulations and IRB procedures
- Exceptional organizational skills with attention to detail
- Excellent communication and stakeholder management abilities
- Ability to manage multiple complex projects simultaneously