Job Description
Job Summary:
We are seeking a highly motivated and experienced contract part-time CRA with a strong background in medical device clinical trials. The ideal candidate will support project setup, site initiation, and administrative processes. A medical or nursing education is preferred, along with hands-on experience in regulatory submissions, budget negotiations, and site management in the medical device industry.
Job Responsibilities:
Ensure clinical trials are conducted in compliance with ISO 14155, ICH-GCP, local regulations, and company SOPs.
Verify data integrity and ensure the rights, safety, and well-being of trial participants are protected.
Conduct study start-up activities, including site initiation and document collection.
Independently perform routine monitoring visits, including site monitoring and close-out visits.
Manage study supplies and ensure appropriate inventory at cl...
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