Job Description
Join our cutting-edge healthcare team at Boston Medical Research Institute, where innovation meets compassionate care. We're seeking a dedicated Senior Clinical Research Coordinator to lead pivotal studies that advance medical treatments and improve patient outcomes. In this role, you'll collaborate with world-class physicians, scientists, and regulatory experts to ensure the integrity and efficiency of clinical trials. Our state-of-the-art facilities and supportive environment provide the perfect platform for professional growth and meaningful impact in the healthcare sector.
Responsibilities
- Design and implement clinical trial protocols in compliance with FDA regulations and ICH-GCP standards
- Manage patient recruitment, screening, and enrollment processes to meet trial timelines
- Oversee data collection, quality control, and regulatory documentation submissions
- Coordinate multidisciplinary teams including physicians, nurses, and data specialists
- Monitor adverse events and ensure participant safety throughout study phases
- Prepare comprehensive trial reports for regulatory bodies and institutional review boards
- Maintain accurate electronic data capture systems and study documentation
Qualifications
- Master's degree in Clinical Research, Nursing, or related health science field
- 5+ years of clinical trial coordination experience with Phase II-III studies
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in FDA 21 CFR Part 312 and ICH-GCP compliance protocols
- Advanced proficiency in electronic data capture systems (e.g., Medidata Rave)
- Proven track record in managing complex multi-site trials
- Exceptional organizational skills with attention to regulatory documentation
- Strong interpersonal skills for effective stakeholder communication