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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

Boston Medical Center
Boston
Salary Estimate
USD 95.000 – USD 120.000
Latest
Live Update
24 Mei 2026
Deadline
24 Mei 2027

Job Description

Join Boston Medical Center's cutting-edge research division and accelerate breakthroughs in patient care. We seek a meticulous Clinical Research Coordinator to orchestrate complex clinical trials while ensuring regulatory excellence and ethical integrity. You'll collaborate with world-class physicians, manage multi-center studies, and contribute to life-changing medical innovations in a dynamic, mission-driven environment.

Our ideal candidate thrives in fast-paced healthcare settings, values precision, and is passionate about translating scientific discoveries into tangible patient outcomes. Enjoy competitive compensation, comprehensive benefits, and unparalleled professional development in Boston's premier academic medical center.

Responsibilities

  • Coordinate end-to-end execution of clinical trials from protocol design to final FDA submission
  • Recruit, screen, and enroll study participants while maintaining strict compliance with HIPAA and GCP standards
  • Manage electronic data capture systems (EDC), ensuring 100% data accuracy and audit readiness
  • Schedule and conduct site visits, monitor adverse events, and prepare regulatory documentation
  • Liaise with sponsors, IRB committees, and external CROs to ensure protocol adherence
  • Maintain meticulous study documentation including case report forms (CRFs) and investigator brochures
  • Mentor junior research staff and train new personnel on SOPs and regulatory requirements

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or related field; Master's preferred
  • Certified Clinical Research Coordinator (CCRC) or ACRP certification required
  • Minimum 3 years of clinical trial coordination experience in oncology or cardiology
  • Expertise in FDA regulations, ICH-GCP guidelines, and 21 CFR Part 11 compliance
  • Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm) and REDCap
  • Exceptional organizational skills with ability to manage 5+ concurrent protocols
  • Strong problem-solving abilities and experience resolving complex regulatory issues

Required Skills

Clinical Trials Regulatory Compliance Data Management Patient Recruitment FDA Regulations GCP EDC Systems IRB Submissions Oncology Cardiology

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