IQVIA LLC is seeking a Lead Medical Writer in the United Kingdom to drive delivery of CSRs, protocols and related documents for clinical research projects. You will lead senior reviews, negotiate timelines with customers, and ensure adherence to IQVIA SOPs and regulatory requirements.
The role requires 5+ years of relevant regulatory writing experience, strong communication skills, and the ability to mentor junior staff while maintaining high-quality deliverables.
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Lead Medical Writer & Project Strategist 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.
