Join our Regulatory Affairs department as a Scientific (Medical) Writing Lead. Position is in any EU country. Scientific Writing Lead prepares clinical and regulatory documentation as a hands-on medical writer, leads and supports the Scientific Writing team operationally and coordinates scientific writing projects.
Requirements
- MSc or higher degree in Medicine, Pharmacy, Public Health or Life Sciences
- PhD degree is preferred but not essential
- At least 5 years experience in medical or scientific writing
- Previous mentoring or line management experience is preferred
- Fluency in native language and English
- In depth knowledge of clinical development process, regulatory procedures, and relevant industry guidelines
- Good understanding of basic human anatomy and physiology
- Basic knowledge of biostatistics
- Scientific writing competency
- Good knowledge of MS Word, Excel, PowerPoint, Outlook, reference management software, etc.
- Continuous professional learning and development
- Attention to details
- Ability to prioritize and work to deadlines with high quality
- Ability to work independently and within the team
Benefits
- International team and environment
- Professional growth and career opportunities
- Bonus based on annual performance
- Additional bonus system – Instant reward and Recognition program
- Personal accident and business trip insurance
- Additional health insurance
- Workplace establishment allowance (only fully home-based)
- Influenza vaccines
- Rewarding referral policy
- Remote work possibility & flexible working hours