Onsite Medical Writing Specialist

Posted 19 hours ago

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About the role

  • Medical Writing Specialist shaping scientific communication across global clinical development. Delivering high-quality clinical documentation and influencing strategic decisions in the pharmaceutical industry.

Responsibilities

  • Deliver a broad range of regulatory medical writing tasks to a consistently high standard
  • Act as Clinical Reporting Project Lead or Medical Writing Lead on assigned projects, ensuring alignment across stakeholders
  • Represent Medical Writing in cross-functional discussions and project groups
  • Share better practices, mentor colleagues, and contribute to capability building
  • Lead process optimisation initiatives and help develop innovative solutions that support our strategic ambitions

Requirements

  • Master’s degree within natural sciences (e.g., M.Sc., M.Sc. Pharm., or equivalent) ideally supplemented with a PhD
  • At least 5 years of relevant medical writing experience in the pharmaceutical industry
  • Expert understanding of clinical development, regulatory requirements, and clinical documentation
  • Full proficiency in written and spoken English

Benefits

  • Health insurance
  • Opportunities to learn and develop

Job title

Medical Writing Specialist

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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