IQVIA is seeking a senior-level FTE Medical Writer to deliver clinical documents including CTRs, IBs, and submissions within sponsor processes. The role emphasizes eye health and inflammation, with collaboration across trial teams and regular training on sponsor SOPs.
The candidate should have strong global regulatory knowledge and 5 years of medical writing experience in biopharma or CRO settings, along with expertise in EDMS and structured authoring tools.
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Senior Medical Writer: Eye Health & Regulatory Submissions in City of Westminster employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.