Job Description:
The CRA position will be responsible for tracking key study metrics, creating and reviewing study related documents, clinical data review, and assisting in vendor management to support the successful execution of clinical trials.
Skills:
Thorough understanding of ICH-GCP guidelines, and FDA regulations, The ability to handle multiple priorities within matrix environment is required, Good computer skills: Word, Excel, PowerPoint, Outlook. Experience with electronic data capture systems a plus, IN HOUSE experience required
Education:
University degree (equal to 4 years of college) in (para-) medical, pharmaceutical, sciences, life-sciences or biosciences. Equally recognized degree and/or relevant qualifications by experience may also be acceptable and will be evaluated on a case-by-case basis.
Remote in NJ: Sr. CRA (232155)
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