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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

Boston Medical Innovations
Boston
Salary Estimate
USD 90.000 – USD 110.000
Live Update
14 Mei 2026
Deadline
15 Mei 2027

Job Description

Join Boston Medical Innovations as a Clinical Research Coordinator and become a pivotal force in transforming healthcare. We're seeking a meticulous professional to orchestrate groundbreaking clinical trials that directly impact patient outcomes. Our state-of-the-art research facility in Boston's Longwood Medical Area offers an unparalleled environment for innovation and collaboration. This role provides the opportunity to work alongside world-class physicians and contribute to life-changing medical advancements while enjoying competitive compensation and comprehensive benefits.

Responsibilities

  • Design, implement, and monitor clinical trial protocols ensuring compliance with FDA regulations and ICH-GCP standards
  • Recruit, screen, and enroll participants while maintaining ethical conduct and patient confidentiality
  • Manage electronic data capture systems, conduct source data verification, and generate comprehensive trial reports
  • Coordinate interdisciplinary teams including physicians, nurses, and biostatisticians to ensure seamless trial execution
  • Prepare regulatory submissions and maintain accurate trial documentation for audit readiness
  • Analyze trial data and contribute to manuscript development for peer-reviewed publications

Qualifications

  • Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
  • Certified Clinical Research Professional (CCRP) or equivalent certification required
  • Minimum 3 years' experience in clinical trial coordination within academic or pharmaceutical settings
  • Expertise in FDA regulations, ICH-GCP, and clinical trial management software (e.g., Medidata Rave)
  • Exceptional organizational skills with ability to manage multiple complex protocols simultaneously
  • Strong written and verbal communication skills for stakeholder interactions and regulatory documentation
  • Proven ability to maintain meticulous records and ensure 100% audit compliance

Required Skills

Clinical Research FDA Regulations GCP Data Management Protocol Design Patient Recruitment Regulatory Compliance Biostatistics Medical Writing

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