Regulatory Medical Writer - London, United Kingdom - X4 Group

X4 Group
X4 Group
Verified Company
London, United Kingdom

1 month ago

Tom O´Connor

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Tom O´Connor

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Description
A global pharmaceutical company are looking for a freelancer to join their team for 6-month project. This role is fully remote and offers a flexible rate dependent on experience.


Job Outline:


  • Authoring regulatory and clinical documents which align with regulatory requirements and project strategies.
  • Creating writing deliverables such as clinical study reports, study protocols, patient information, informed consent forms, integrated summary reports, investigator brochures and other medical and regulatory documents.
  • Keep management informed on progress of documents and other projectrelated information.

Requirements:


  • Bachelor's degree in the life sciences; MS or PhD preferred.
  • Extensive experience in the writing regulatory documents for pharmaceutical, biologic or medical device companies.
  • Great understanding of the clinical drug development process.
  • Highly organised; able to achieve goals, working to strict timelines.

LinkedIn:
Dzestina Janarauskaite | LinkedIn
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