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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

Boston Medical Innovations
Boston
Salary Estimate
USD 85.000 – USD 110.000
Live Update
24 Mei 2026
Deadline
24 Mei 2027

Job Description

Join our pioneering team at Boston Medical Innovations, where cutting-edge healthcare meets transformative research. We're seeking a Clinical Research Coordinator to drive critical medical studies that shape the future of patient care. This role offers the opportunity to work alongside world-class physicians in a collaborative, mission-driven environment while contributing to breakthrough treatments.

Our comprehensive benefits package includes health insurance, retirement matching, and professional development stipends. We offer flexible scheduling and hybrid work options to support work-life balance. Boston Medical Innovations is committed to diversity, equity, and inclusion in all aspects of our operations.

Responsibilities

  • Manage clinical trial protocols ensuring compliance with FDA regulations and institutional guidelines
  • Recruit, screen, and enroll participants while maintaining detailed study documentation
  • Coordinate multi-disciplinary research teams including physicians, nurses, and data specialists
  • Monitor adverse events and ensure timely regulatory reporting
  • Develop and maintain study budgets, timelines, and resource allocation plans
  • Analyze clinical data and prepare comprehensive reports for stakeholders
  • Represent the organization at industry conferences and regulatory meetings

Qualifications

  • Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
  • 3+ years of clinical research coordination experience with FDA-regulated trials
  • Certified Clinical Research Professional (CCRP) certification required
  • Proficiency with electronic data capture systems (e.g., Medidata Rave)
  • Demonstrated knowledge of ICH-GCP and 21 CFR regulations
  • Exceptional organizational skills with attention to detail
  • Strong written and verbal communication abilities
  • Experience with oncology trials highly desirable

Required Skills

Clinical Research Regulatory Compliance Data Management IRB Protocol Development Patient Recruitment Medical Terminology FDA Regulations Clinical Trials Oncology

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