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Principle Medical Writer – Leading CRO, Manchester
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Client:
Carrot Recruitment
Location:
Manchester, United Kingdom
Job Category: Work abroad Healthcare
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EU work permit required:
Yes
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Job Reference:
f50f8912e0bd
Job Views:
13
Posted:
26.04.2025
Expiry Date:
10.06.2025
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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 Report, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical Overviews etc and more
* Managing multiple projects concurrently, taking the lead on projects
* Mentoring junior members of the team
* Reviewing all documentation to a high standard
* Working across multiple therapy areas
* Meet both internal/external deliverables against set timelines
You
To apply for this role as Principal Medical Writer (Regulatory / Clinical) our client is hoping for someone with the following skills and experience;
* Ample experience in a Medical Writing / Regulatory Writing role
* Experienced within a CRO or Pharma setting
* Experienced writing, editing, and reviewing documents such as Clinical Study Report, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical Overviews
* Can work in a fast-paced environment, meeting internal and external deliverables
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Created on 26/04/2025 by TN United Kingdom
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