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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

Boston Medical Center
Boston
Salary Estimate
USD 85.000 – USD 110.000
Live Update
11 Mei 2026
Deadline
11 Mei 2027

Job Description

Join Boston Medical Center's pioneering research division as a Clinical Research Coordinator and drive transformative healthcare innovation. We're seeking a detail-oriented professional to manage groundbreaking clinical trials that directly impact patient outcomes and advance medical science. This hybrid role offers the unique opportunity to work at the intersection of cutting-edge research and compassionate patient care in one of America's top medical institutions.

Why BMC? As an academic medical center, we provide unparalleled resources for professional growth, state-of-the-art research facilities, and a collaborative environment where your contributions shape the future of medicine. Enjoy comprehensive benefits including tuition assistance, wellness programs, and competitive retirement plans.

Responsibilities

  • Design, implement, and monitor clinical trial protocols ensuring compliance with FDA regulations and GCP standards
  • Coordinate patient recruitment, enrollment, and retention strategies for diverse study populations
  • Manage comprehensive data collection, quality control, and regulatory documentation processes
  • Serve as primary liaison between investigators, sponsors, IRB, and study participants
  • Oversee study budgets, vendor contracts, and financial reconciliation
  • Train and mentor clinical research staff on protocol procedures and regulatory requirements
  • Analyze trial data and prepare comprehensive reports for regulatory submissions

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
  • Certified Clinical Research Professional (CCRP) or equivalent certification required
  • Minimum 3 years experience in clinical research coordination with FDA-regulated trials
  • Proven expertise in electronic data capture systems (e.g., REDCap, Medidata Rave)
  • Exceptional organizational skills with meticulous attention to documentation
  • Strong interpersonal abilities to communicate complex protocols to diverse audiences
  • Experience with IRB submissions and regulatory compliance management
  • Demonstrated problem-solving skills in resolving protocol deviations and data discrepancies

Required Skills

Clinical Research FDA Regulations GCP IRB Data Management Patient Recruitment REDCap Regulatory Compliance

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