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Clinical Research Coordinator

Boston Medical Innovations
Boston, MA
Salary Estimate
USD 85.000 – USD 110.000
Latest
Live Update
25 Mei 2026
Deadline
25 Mei 2027

Job Description

Join our pioneering medical research team at Boston Medical Innovations, where cutting-edge science meets compassionate care. We're seeking a Clinical Research Coordinator to drive transformative clinical trials that shape the future of medicine. In this pivotal role, you'll collaborate with world-class physicians, scientists, and regulatory experts to ensure seamless execution of groundbreaking studies. Our state-of-the-art facilities in Boston's renowned Longwood Medical Area provide an unparalleled environment for innovation. Enjoy competitive compensation, comprehensive benefits, and the opportunity to make a tangible impact on global health outcomes.

Responsibilities

  • Design, implement, and oversee clinical trial protocols in compliance with FDA regulations and ICH-GCP standards
  • Recruit, screen, and enroll study participants while maintaining ethical research practices
  • Manage comprehensive electronic data capture systems ensuring accuracy and regulatory compliance
  • Coordinate multidisciplinary research teams including physicians, nurses, and biostatisticians
  • Prepare regulatory submissions and maintain meticulous documentation for audits
  • Analyze and interpret clinical data to generate actionable insights for study leadership
  • Represent the organization at investigator meetings and scientific conferences

Qualifications

  • Master's degree in Clinical Research, Public Health, or related life sciences field
  • 3+ years of clinical trial coordination experience in a hospital or pharmaceutical setting
  • Certified Clinical Research Professional (CCRP) or equivalent certification preferred
  • Expertise in FDA regulations, ICH-GCP, and 21 CFR Part 11 compliance
  • Proficiency in electronic data capture systems (e.g., Medidata Rave, Oracle Inform)
  • Exceptional organizational skills with meticulous attention to documentation
  • Strong written and verbal communication abilities for diverse stakeholder interactions
  • Ability to manage competing priorities in a fast-paced research environment

Required Skills

Clinical Trials Regulatory Compliance Data Management Patient Recruitment FDA Regulations IRB Protocols Medical Terminology Research Methodology

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