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Clinical Trials Medical Writer

Rochester Regional Health • Rochester, NY, US • published 2026-10-16 02:18:53.724456

Description

**Job Title:** Medical Writer **Department:** Study Set Up **Location:** Remote East Coast \| Must Sit in East Coast **Hours Per Week:** 40 hours **Schedule:** Days, Monday – Friday **SUMMARY** The Medical Writer is responsible for interpreting complex clinical study protocols and other medical/scientific documentation to prepare and coordinate laboratory specification and study‑specific medical/technical documents for ACM Global Laboratories. They will partner with internal departments in the development, drafting, review, editing, and finalization of documents used to conduct clinical studies. **RESPONSIBILITIES** * Lead the development, revision, and maintenance of complex clinical study and amendments in accordance to standard operating procedures (SOPs) and regulatory requirements. * With support of a mentor, work on the development, revision, and maintenance of high profile and expedited complex study documents and amendments in accordance to SOPs and regulatory requirements. * Responsible for authoring and finalizing global lab specification documents (GLSD) and other related documents, as needed. * Interpret, understand, and contribute to the scientific details of the proto...

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