Job Description
Join our pioneering team at MediCore Research Institute, where innovation meets compassionate care. We're seeking a Senior Clinical Research Coordinator to drive cutting-edge clinical trials that transform patient outcomes in oncology and rare diseases. In this pivotal role, you'll manage complex study protocols, collaborate with multidisciplinary teams, and ensure compliance with FDA and ICH-GCP standards. Our state-of-the-art facilities in Boston's medical district offer unparalleled resources for career growth and impact.
Responsibilities
- Oversee end-to-end clinical trial execution from protocol design to final report submission
- Recruit and retain diverse patient populations while maintaining ethical standards
- Monitor trial progress through EDC systems, identifying risks and implementing corrective actions
- Train and mentor junior staff on regulatory compliance and study procedures
- Liaise with sponsors, IRBs, and investigative sites to ensure seamless trial operations
- Analyze and interpret clinical data to support publication-ready manuscripts
Qualifications
- Master's degree in Nursing, Public Health, or related clinical field
- 5+ years of clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in clinical trial management systems (e.g., Medidata Rave, Veeva Vault)
- Demonstrated success in achieving 95%+ patient retention rates
- Strong knowledge of 21 CFR Part 11, ICH-GCP, and FDA regulations
- Exceptional written and verbal communication skills for stakeholder reporting