Join the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence, as a Senior Medical Writer.
In this role, you will support a Top-5 pharma company, helping deliver best-in-class regulatory and submission documents. You will be fully embedded with our client while being employed by ICON.
Responsibilities :
* Independently produce clinical and regulatory documents in collaboration with Principal Medical Writers. These may include Clinical Study Protocols and Clinical Study Reports across Phase 1 to Phase 3 in multiple therapeutic areas.
* Analyze and interpret data thoroughly to determine the best approach for document composition, applying lean writing strategies.
* Serve as the primary contact for the study team regarding preparation and timelines of assigned documents, including planning.
* Facilitate document reviews, ensuring they are submission-ready and approved, working closely with QC personnel and publishing specialists.
Minimum Requirements :
* 3-5 years of Medical Writing or relevant pharmaceutical experience with scientific and regulatory knowledge.
* Strong writing skills with the ability to convert scientific data into clear, well-structured messages.
* Proficient in independently writing various clinical / regulatory documents, mainly CSRs and Protocols, including leading creation, coordination, review facilitation, and ensuring submission readiness.
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