ProPharma is seeking a Senior/Principal Medical Writer to join its FSP Medical Writing group in the UK or Ireland. The role focuses on authoring high-quality clinical and regulatory documents across phases, with early-phase experience preferred.
You will coordinate with cross-functional teams, mentor junior writers, and ensure timely delivery within budget. The successful candidate will have at least 5 years in medical writing for drugs, biologics, or devices, strong FDA/regulatory knowledge,
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Senior Medical Writer – Early-Phase & Regulatory Lead employer: ProPharma
ProPharma is an exceptional employer that fosters a culture of diversity, equity, and inclusion, empowering employees to be their authentic selves while driving innovation in the healthcare sector. With a commitment to employee growth, ProPharma offers opportunities for professional development and collaboration, particularly in its Eastern European hubs, where remote work is supported alongside hybrid office engagement. Join us to make a meaningful impact in the field of compliance and quality assurance, all while enjoying a supportive and dynamic work environment.
