Clinical Protocol Writer - Trials & Regulatory Docs
Speros
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.
#J-18808-LjbffrVacancy posted 4 days ago
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