Job Description
Join MedTech Innovations as a Clinical Research Coordinator and drive breakthroughs in medical science. We're a cutting-edge healthcare research firm dedicated to transforming patient outcomes through innovative clinical trials. Our Boston-based team operates at the intersection of technology and medicine, offering a collaborative environment where your expertise directly impacts global health initiatives.
As a key member of our research division, you'll manage complex clinical trials from protocol development to final analysis, ensuring compliance with FDA regulations and ethical standards. We provide comprehensive training, competitive benefits, and opportunities for professional growth in one of America's premier healthcare hubs.
Responsibilities
- Design and oversee clinical trial protocols in collaboration with multidisciplinary research teams
- Recruit, screen, and enroll participants while maintaining strict regulatory compliance
- Manage trial budgets, vendor contracts, and regulatory documentation
- Analyze clinical data and prepare comprehensive reports for stakeholders
- Coordinate with IRB/ethics committees and ensure protocol adherence
- Maintain accurate electronic trial records in compliance with 21 CFR Part 11
- Liaise with pharmaceutical partners and regulatory agencies throughout trial phases
Qualifications
- Bachelor's degree in Nursing, Biology, or related health science field (Master's preferred)
- Minimum 3 years of clinical research coordination experience
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Proficiency in EDC systems (e.g., Medidata Rave, Oracle Inform)
- Deep knowledge of FDA regulations, GCP, and ICH guidelines
- Exceptional organizational skills with attention to detail
- Strong written communication abilities for regulatory documentation
- Experience managing oncology or cardiovascular trials highly desirable