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Senior Director

2 months ago

København, Denmark iPowerPartner Full time

Being an experienced global solutions agency, iPower Partner helps organizations transform in a fast-changing market by providing a full consultation package of company registration/ business license, representative office setup, visa & work permit, and RPO/Headhunting that enables them to win. Our team has international connections, regional knowledge and local market experience - strengthening our partnerships with multinational blue-chip corporations and local companies in Asia and Europe, to provide them with top-notch services while finding sustainable employment for people across a wide range of industries and skills.

_Our partner is a top-tier Biotechnology company in healthcare based in Copenhagen, Denmark. We are searching for a highly motivated Senior Director in Medical Writing to strengthen its leadership team either in Copenhagen or Amsterdam. Your responsibilities include planning, developing, and writing clinical documents to support medical and regulatory activities across the product portfolio.

Ideal candidates possess a Life Sciences degree, a broad background, and solid knowledge of clinical drug development and regulatory requirements._

Tasks
  • Lead planning and authoring of complex clinical and regulatory documents.
  • Guide medical writing and project teams during the planning and authoring stages.
  • Drive strategic medical writing initiatives and processes.
  • Contribute to/lead Medical Writing digitalization efforts.
  • Lead development, review, and improvement of departmental processes.
  • Coordinate with the Technical Document Manager and Document Quality Control groups.
  • May oversee medical writing vendors/CROs.
  • Proactively engage in department activities and mentor junior writers.
  • Provide input to the overall strategy and development of the Medical Writing department.
Requirements
  • At least BA/BS degree in Life Sciences
  • 13+ years of medical or scientific writing experience in the pharmaceutical industry.
  • Oncology and immunology experience is a must
  • Extensive experience in writing various clinical documents and regulatory filings.
  • Expert understanding of regulatory requirements, drug development processes, and Good Clinical Practice.
  • Proficiency in document content preparation and interpreting complex data presentations.
  • Proficiency in relevant software.
Benefits
  • Market competitive compensation package including performance-based annual bonus scheme
  • Company shares (generous welcome grant and performance-based annual equity plan)
  • In-house and external learning and development opportunities
  • Fantastic benefits program and keep improving
  • Plus you get to work with a dynamic team of collaborative, supportive, inclusive, and fun professionals whose mission is clear: Cancer has no borders and neither do we.
  • Join us and Make momentum in your career
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