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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

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

Job Description

Join Boston Medical Innovations, a leader in cutting-edge clinical research, as we pioneer breakthrough treatments in oncology and rare diseases. We seek a meticulous Clinical Research Coordinator to drive our mission of transforming patient outcomes through rigorous scientific inquiry. This pivotal role offers the opportunity to work alongside world-renowned physicians and scientists in a collaborative, intellectually stimulating environment. Enjoy competitive compensation, comprehensive benefits, and the chance to make a tangible impact on global healthcare.

Responsibilities

  • Design, implement, and oversee clinical trial protocols ensuring compliance with FDA regulations and ICH-GCP standards
  • Coordinate patient recruitment, enrollment, and retention activities while maintaining ethical trial conduct
  • Manage comprehensive documentation including case report forms, informed consent, and regulatory submissions
  • Liaise with multidisciplinary teams (physicians, nurses, statisticians) to ensure seamless trial execution
  • Monitor adverse events and ensure patient safety throughout the research process
  • Analyze and interpret clinical data to generate actionable insights for study teams
  • Maintain regulatory documentation and communicate findings to internal and external stakeholders

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
  • 3+ years of clinical research coordination experience in oncology or rare disease trials
  • Certified Clinical Research Professional (CCRP) or equivalent certification required
  • Proven expertise in FDA/ICH-GCP regulations and institutional review board (IRB) processes
  • Exceptional organizational skills with meticulous attention to documentation
  • Strong analytical abilities for data interpretation and protocol development
  • Excellent communication skills for stakeholder collaboration and patient interactions
  • Experience with electronic data capture systems (EDC) and clinical trial management software

Required Skills

Clinical Research Regulatory Compliance Data Management Patient Recruitment Ethics GCP Medical Terminology Communication

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