Senior Medical Writer & Regulatory Submissions Lead
Listed on 2026-10-06
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IT/Tech
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Research/Development
IQVIA is seeking an experienced Principal Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role will ensure documents such as Investigator’s Brochures, Clinical Study Reports, and Module II summaries are scientifically accurate and compliant with global guidelines.
The successful candidate will serve as the lead writer for key summary documents, guiding cross-functional teams while overseeing medical writing
This posting is for the Senior Medical Writer & Regulatory Submissions Lead role at IQVIA, based in Durham, NC, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Medical Writer & Regulatory Submissions Lead role in the description above.
We appreciate your interest in this position.
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