The Medical Writer is responsible for supporting the clinical research program by collaborating with Principal Investigators (PIs) and study-related individuals to write clinical trial protocols, informed consent documents, and other study-related documents. The Medical Writer will be integrally involved with the writing and editing of clinical study reports and study-related journal articles in support of investigator initiated research, and other documents as needed.
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Job Type
Full-time
Career Level
Mid Level
Industry
Hospitals
Education Level
Master's degree