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Clinical Protocol Writer – Trials & Regulatory Docs
Job in
Northern, Floyd County, Kentucky, USA
Listed on 2026-08-23
Listing for:
SPEROS
Full Time
position Listed on 2026-08-23
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Research Scientist, Medical Science
Job Description & How to Apply Below
Moffitt Cancer Center in Florida seeks a clinical research Protocol Writer to collaborate with clinical investigators to write, edit and complete clinical trial protocols and related documents for SRC submissions. Under the PI, you will gather technical and scientific materials to conceptualize and deliver proposals.
This role requires deadline-driven organization and ability to manage multiple projects, with 2+ years medical writing experience and a strong background in regulatory documents.
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