Job Description
Join Boston Medical Innovations as a Clinical Research Coordinator and become a vital force in advancing medical breakthroughs. We're seeking a detail-oriented professional to orchestrate complex clinical trials that shape the future of patient care. In this pivotal role, you'll collaborate with multidisciplinary teams to ensure regulatory compliance, data integrity, and seamless participant experiences while contributing to life-changing therapies.
Our state-of-the-art research facility in Boston's renowned Medical Mile offers unparalleled resources and a culture where innovation meets compassion. Enjoy competitive benefits, professional development opportunities, and the satisfaction of directly impacting healthcare outcomes.
Responsibilities
- Design and execute comprehensive clinical trial protocols in alignment with FDA/ICH-GCP standards
- Recruit, screen, and enroll study participants while maintaining strict ethical guidelines
- Manage electronic data capture systems and ensure accurate documentation of trial progress
- Serve as primary liaison between investigators, sponsors, and regulatory bodies
- Monitor adverse events and ensure timely reporting to institutional review boards
- Analyze clinical data and prepare comprehensive reports for stakeholder reviews
- Maintain meticulous trial documentation and regulatory compliance files
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in therapeutic areas
- Certified Clinical Research Professional (CCRP) certification required
- Proficiency in clinical trial management systems (e.g., Medidata Rave, Veeva Vault)
- Deep understanding of FDA regulations and Good Clinical Practices
- Exceptional organizational skills with attention to regulatory documentation
- Strong written and verbal communication abilities for stakeholder interactions
- Experience with IRB submissions and protocol development