Principle Medical Writer – Leading CRO

TN United Kingdom; Manchester; On-site; GBP 45,000 - 70,000; Full time

Job summary

An established industry player is seeking a Principal Medical Writer to join their dynamic team in Manchester. This exciting role involves writing, editing, and reviewing critical regulatory documents while managing multiple projects across various therapy areas. The ideal candidate will have substantial experience in a Medical Writing role within a CRO or Pharma setting. You'll have the opportunity to mentor junior team members and ensure high-quality documentation is delivered on time. Join a forward-thinking company and contribute to impactful healthcare projects that make a difference!

Qualifications

• Ample experience in a Medical Writing / Regulatory Writing role.
• Experienced in writing and reviewing clinical documents.

Responsibilities

• Write and review clinical documents such as protocols and reports.
• Manage multiple projects and mentor junior team members.

Skills

Medical Writing

Regulatory Writing

Clinical Study Report

Editing and Reviewing

Project Management

Mentoring

Job description

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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