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Senior Medical Writer
ICON plc
Frankfurt +9 · RemoteMid level (2–5 years)Full-timePosted 28 days ago
About the job
What you'll do
Independently develop clinical and regulatory documents, including study protocols and reports, by critically interpreting clinical data and coordinating document planning, review, and approval. Serve as the primary writing contact for study teams and mentor junior medical writers.
What they're looking for
Requires 3–5 years of regulatory writing experience, including mandatory Phase II or III protocol-writing experience; clinical study report experience is preferred. Applicants need a relevant bachelor's degree, strong clinical data interpretation and writing skills, knowledge of ICH-GCP, FDA, and EMA requirements, and effective communication and collaboration skills.
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