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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

MedTech Innovations
Boston
Salary Estimate
USD 90.000 – USD 120.000
Live Update
27 Mei 2026
Deadline
27 Mei 2027

Job Description

Join our pioneering medical research team at MedTech Innovations, where cutting-edge science meets compassionate care. We're seeking a Clinical Research Coordinator to drive groundbreaking studies that transform patient outcomes in oncology and rare diseases. Work alongside world-class physicians in our state-of-the-art Boston facility while contributing to therapies that save lives.

Why Join Us?

  • Competitive salary with comprehensive benefits package
  • Access to industry-leading medical technology and resources
  • Professional development through conferences and certifications
  • Collaborative environment with flexible work arrangements

Responsibilities

  • Design and implement comprehensive clinical trial protocols aligned with FDA regulations
  • Recruit, screen, and enroll qualified participants while maintaining ethical standards
  • Monitor patient progress and adverse events through electronic health records
  • Coordinate multidisciplinary teams including physicians, nurses, and data specialists
  • Prepare regulatory submissions and ensure protocol compliance
  • Analyze trial data and generate detailed reports for stakeholders
  • Maintain accurate documentation in compliance with 21 CFR Part 11

Qualifications

  • Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
  • Certified Clinical Research Professional (CCRP) or equivalent certification
  • Minimum 3 years clinical trial coordination experience in oncology
  • Proficiency with EDC systems (e.g., Medidata Rave, Oracle Inform)
  • Strong knowledge of ICH-GCP and FDA regulations
  • Exceptional interpersonal skills for patient engagement and team leadership
  • Detail-oriented with excellent data management abilities
  • Valid CPR certification and ability to work flexible hours

Required Skills

Clinical Trials FDA Regulations Patient Recruitment EDC Systems Data Management Oncology ICH-GCP Protocol Design

Ready to Take on This Challenge?

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