MMS in Manchester seeks a full-time Medical Writer to write and edit clinical development documents. The role involves critically evaluating medical literature, maintaining timelines, and mentoring team members. Ideal candidates have 3-5 years in regulatory and clinical writing, with a strong background in clinical study protocols. Proficiency in MS Office tools is required. Join MMS, an award-winning CRO and part of an inclusive team shaping the future of clinical research.
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