Principle Medical Writer – Leading CRO

Principle Medical Writer – Leading CRO, Manchester Client: Carrot Recruitment Location: Manchester, United Kingdom Job Category: Other – EU work permit required: Yes Job Reference: f50f8912e0bd Job Views: 4 Posted: 02.06.2025 Expiry Date: 17.07.2025 Job Description: The Role Working on a number of exciting projects and with an exciting pipeline, the Principal Medical Writer (Regulatory) will be responsible for: Writing, editing, and reviewing documents such as Clinical Study Reports, Protocols, Informed Consent forms, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections, and Clinical Overviews. Managing multiple projects concurrently, taking the lead on projects. Mentoring junior team members. Reviewing all documentation to a high standard. Working across multiple therapy areas. Meeting internal and external deliverables within set timelines. You To apply for this role as Principal Medical Writer (Regulatory / Clinical), our client is looking for someone with: Extensive experience in Medical Writing / Regulatory Writing roles. Experience within a CRO or pharmaceutical setting. Proven ability to write, edit, and review documents such as Clinical Study Reports, Protocols, Informed Consent forms, Safety Reports, and Clinical Summaries. The ability to work in a fast-paced environment, meeting tight deadlines. #J-18808-Ljbffr