Contract Medical Writer

August 17

🏡 Remote – New York

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Logo of AL Solutions

AL Solutions

A global headhunting team supporting the Life Science industry across the UK, EU, USA.

trials • consulting • health economics • market access • clinicalresearch

11 - 50

Description

• Serve as primary author for complex regulatory/clinical documentation • Author/Co-authoring of IND's, BLA's, CSR's, Protocols & IB's • Writing, reviewing & editing of scientific early-phase clinical documentation • Cross-functional collaboration with Safety & Regulatory

Requirements

• 5 years experience as a primary author of documents such as IND's, CSR's & Protocols • Oncology experience preferred • Prior experience working with milestones & timelines • Degree in Life Sciences

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