Principle Medical Writer – Leading CRO

Carrot Recruitment; Manchester; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading CRO in Manchester is seeking a Principal Medical Writer to oversee exciting projects. The role requires extensive experience in medical writing, managing multiple projects, and mentoring team members. It's an opportunity to contribute significantly to the regulatory writing process across various therapy areas.

Qualifications

• Extensive experience in Medical Writing / Regulatory Writing roles.
• Experience within a CRO or pharmaceutical setting.
• Proven ability to write, edit, and review clinical documents.

Responsibilities

• Writing, editing, and reviewing various clinical documents.
• Managing multiple projects and mentoring junior team members.
• Ensuring documentation meets high standards and deadlines.

Skills

Medical Writing

Regulatory Writing

Document Review

Project Management

Mentoring

Job description

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.