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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

Boston Medical Research Institute
Boston
Salary Estimate
USD 85.000 – USD 110.000
Live Update
12 Mei 2026
Deadline
12 Mei 2027

Job Description

Join our pioneering team at Boston Medical Research Institute, where innovation meets compassionate care. We're seeking a Clinical Research Coordinator to drive impactful clinical trials that shape the future of medicine. Work alongside world-class physicians in state-of-the-art facilities while advancing patient-centered therapies. Enjoy competitive benefits, professional development opportunities, and the chance to make a tangible difference in global healthcare outcomes.

Responsibilities

  • Design, implement, and monitor Phase I-III clinical trials ensuring protocol adherence and regulatory compliance
  • Recruit, screen, and enroll eligible participants while maintaining comprehensive study documentation
  • Coordinate multidisciplinary teams including physicians, nurses, and data specialists
  • Manage electronic data capture systems and maintain accurate patient records per FDA/ICH-GCP standards
  • Prepare regulatory submissions and ensure ongoing compliance with institutional review board protocols
  • Analyze trial data and prepare interim/final reports for sponsors and stakeholders
  • Mentor junior research staff and contribute to process improvement initiatives

Qualifications

  • Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
  • 3+ years clinical research coordination experience with therapeutic area specialization
  • Certified Clinical Research Professional (CCRP) or equivalent certification required
  • Proficiency in REDCap, Medidata Rave, or similar EDC platforms
  • Demonstrated knowledge of FDA 21 CFR Part 312/812 and ICH-GCP guidelines
  • Exceptional organizational skills with attention to detail and documentation accuracy
  • Strong interpersonal abilities for patient engagement and team collaboration
  • Experience with IRB submissions and audit readiness preparation

Required Skills

clinical trials regulatory compliance data management patient recruitment FDA regulations EDC systems GCP protocol development

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