Clinical Research Associate

2 weeks ago


Bristol, Maine, United States Medpace Full time
Job Summary

We are seeking a highly experienced Clinical Research Associate to join our Clinical Operations team in South Korea. This role is crucial in ensuring the success of our clinical trials and projects. If you are passionate about using your expertise to drive research and development, this is an exciting opportunity for you.

Responsibilities
  • Verify the accuracy and completeness of trial data, ensuring compliance with regulatory requirements and approved protocols.
  • Conduct site qualification, study initiation, and monitoring visits to ensure site compliance with Medpace and Sponsor Standard Operating Procedures.
  • Collaborate with cross-functional teams to ensure effective working relationships and quality completion of visit reports and study-related databases.
  • Maintain close relationships with clinical investigators and site staff to ensure successful trial execution.
Qualifications
  • Bachelor's degree in a health or science-related field and at least 1-5 years of experience in clinical monitoring.
  • Comprehensive knowledge of clinical monitoring practices and procedures, including practical application.
  • Demonstrated ability to act as a Lead CRA and facilitate training and mentorship for new CRAs.
About Medpace

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.

Why Medpace?

At Medpace, we value our employees' expertise and empower them to take an assertive approach to research and problem-solving. We offer a competitive compensation and benefits package, flexible work schedule, and opportunities for professional growth and development.



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