Senior Regulatory and Medical Writer

Be among the first applicants.
TN United Kingdom
London
Remote
GBP 55,000 - 70,000
Be among the first applicants.
4 days ago
Job description

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Senior Regulatory and Medical Writer, London

Client:

CK Group

Location:

London, United Kingdom

Job Category:

-

EU work permit required:

Yes

Job Reference:

b579688a753a

Job Views:

2

Posted:

28.03.2025

Expiry Date:

12.05.2025

Job Description:

CK Group are recruiting for a Senior Regulatory and Medical Writer to join a leading, dynamic and fast-growing consultancy on a permanent basis. They specialise in Advanced Therapies and Rare Diseases. This will be a fully remote role and candidates looking for permanent, contract or part-time roles will be considered.

RESPONSIBILITIES:
Working as part of the medical writing team, you will be supporting the regulatory affairs, clinical operations and medical affairs teams across a range of projects, and directly with clients for standalone medical writing projects.

  • Preparation of clinical documents such as clinical study protocols and amendments, clinical study reports, and investigator’s brochures/investigator’s brochure updates.
  • Preparation of EU and US regulatory documents.
  • Project management.
  • Managing the document review process.
  • Organizing the quality control (QC) review of documents and addressing QC comments.
  • Editorial support and formatting of documents authored by other team members as required.
  • Peer review of documents authored by other colleagues.
  • Providing guidance and training to less experienced medical writers and members of the wider team.
QUALIFICATIONS:
  • Proven experience gained in a consultancy environment, with a minimum of a B.Sc. in a life sciences subject (a higher degree would be a distinct advantage).
  • Excellent written and verbal communication skills, including the ability to articulate ideas clearly, engage with diverse audiences, and produce error-free written content.
  • Proficient in Microsoft Office with excellent skills in Word.
  • Experience in preparing clinical documents.
  • Significant experience with the preparation of EU and US regulatory documents would be a distinct advantage.
  • Project management skills, including the creation and maintenance of project timelines and liaison with clients.
BENEFITS:
Salary of up to £70,000 plus benefits package.
APPLY:
Please quote job reference 112 567 in all correspondence.
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