Principle Medical Writer – Leading CRO, Manchester
Client: Carrot Recruitment
Location: Manchester, United Kingdom
Job Category: Other
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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.
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