Being an experienced global workforce solutions agency, iPower helps organizations transform in a fast-changing labor market by sourcing, matching, and developing the right talent 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 skilled talent while finding sustainable employment for people across a wide range of industries and skills.
We develop innovative solutions for many companies every year, specializing in Permanent Recruitment, Temporary/ Contract Staffing, Mass Recruitment, and Global Mobility. We offer a unique, consultative approach to recruitment, tailoring every solution to specific requirements and offering long-term support. Through experience, growth and consistently high standards, we have built a reputation for being one of the most reliable partners, confirming our position as the most admired brand in the industry.
Find out more by getting in touch with our team: https://ipowerpartner.com/
Ipower Partner is partnering with 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.
RESPONSIBILITIES
- 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
- 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.
APPLICATION: Interested candidates please click on the APPLY BUTTON to send your resume or contact our consultant, Hung Nguyen for further information: E: hung.nguyen@ipowerpartner.com; T: +84 362166061