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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

Mayo Clinic
Rochester
Salary Estimate
USD 85.000 – USD 110.000
Live Update
12 Mei 2026
Deadline
12 Mei 2027

Job Description

Join Mayo Clinic's world-renowned research team as a Clinical Research Coordinator. You'll play a pivotal role in advancing medical breakthroughs while ensuring the highest standards of patient care and regulatory compliance. This position offers unparalleled opportunities to work alongside leading experts in cutting-edge clinical trials across diverse therapeutic areas.

Mayo Clinic provides a collaborative environment where innovation meets compassionate care. We offer competitive benefits, professional development opportunities, and the chance to make a meaningful impact on global healthcare outcomes. Our Rochester campus features state-of-the-art facilities and a commitment to excellence in medical research.

Responsibilities

  • Oversee all aspects of clinical trial execution including protocol implementation, patient recruitment, and data management
  • Ensure strict adherence to FDA regulations, GCP guidelines, and institutional IRB requirements
  • Coordinate with multidisciplinary teams including physicians, nurses, and biostatisticians
  • Manage regulatory documentation, informed consent processes, and adverse event reporting
  • Maintain accurate trial documentation and electronic data capture systems
  • Monitor patient safety and protocol compliance throughout study duration
  • Participate in site initiation visits, audits, and regulatory inspections

Qualifications

  • Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
  • Minimum 2 years clinical research coordination experience with FDA-regulated trials
  • Certified Clinical Research Professional (CCRP) or equivalent certification
  • Expert knowledge of ICH-GCP, FDA regulations, and clinical trial methodologies
  • Strong data management skills with experience in electronic systems like Medidata Rave
  • Exceptional organizational abilities with attention to detail and documentation accuracy
  • Excellent communication skills for patient interactions and team collaboration
  • Ability to manage multiple protocols and meet critical deadlines

Required Skills

Clinical Trials FDA Regulations GCP IRB Data Management Patient Recruitment Regulatory Compliance Medical Terminology

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