IQVIA is seeking a full-time Medical Writer to deliver clinical documents including CTRs, TDOs/CTPs, IBs, and submission materials. You will be embedded in sponsor processes and use their SOPs to ensure timely, high-quality deliverables across eye health and inflammation programs.
Ideal candidates have about 5 years of medical writing experience in biopharma, biotech, or CRO settings, with strong regulatory knowledge and excellent communication. Proficiency in Word and eDMS is required.
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Senior Medical Writer: Eye Health & Regulatory Docs employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
