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Senior Medical Writer

WALKER COLE INTERNATIONAL LTD
Posted 20 hours ago, valid for 7 days
Location

London, Greater London EC1R 0WX

Salary

£40,000 - £48,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Walker Cole International is looking for a Senior Medical Writer to join a UK-based pharmaceutical company that specializes in immunotherapy, working remotely.
  • The role requires extensive experience in medical writing within the pharmaceutical or biotech industry, specifically with a focus on writing essential clinical documents.
  • Key responsibilities include developing Investigator Brochures, study protocols, and Clinical Study Reports to support clinical development and regulatory submissions.
  • Candidates should hold a master’s degree in a relevant scientific field and have proven experience in authoring key clinical documents for Phase 1-3 studies.
  • The position offers a competitive salary, though the exact figure is not specified, and candidates should possess significant experience in the medical writing domain.

Walker Cole International is seeking a Senior Medical Writer to work remotely for a UK-based pharmaceutical company specializing in immunotherapy.

In this role, you will support the Research and Development (R&D) department by handling all medical writing tasks.

Your key responsibilities will include:

  • Writing and developing essential clinical documents such as Investigator Brochures (IBs), study protocols, and Clinical Study Reports (CSRs) to support clinical development.
  • Organizing and compiling data for clinical documents like the Investigational Medicinal Product Dossier (IMPD) and contributing to the clinical sections of Common Technical Document (CTD) modules.
  • Assisting with clinical publications (e.g. abstracts, posters, manuscripts).
  • Ensuring timely completion of all writing projects to support R&D objectives and facilitate the submission of regulatory dossiers.

Key qualifications for the role include:R

  • A master’s degree in a relevant scientific field.
  • Extensive experience in medical writing within the pharmaceutical or biotech industry.
  • Proven ability to author and edit key clinical documents such as protocols and CSRs for Phase 1-3 studies.
  • Familiarity with therapeutic areas like allergy immunotherapy or respiratory conditions.

Medical Writing | Pharmaceutical | Biotech | Scientific Writing | Medical Affairs | CSR | IB | CTD | Protocol | Clinical Documents | Clinical Trials | Immunotherapeutics | Research & Development | Medical Communications

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.