A global headhunting team supporting the Life Science industry across the UK, EU, USA.
trials • consulting • health economics • market access • clinicalresearch
August 17
🏡 Remote – Anywhere in California
A global headhunting team supporting the Life Science industry across the UK, EU, USA.
trials • consulting • health economics • market access • clinicalresearch
• 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
• 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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