Scientific (Medical) Writing Lead job opportunity at Biomapas.

Home Jobs In Czechia Tag: Job Scientific (Medical) Writing Lead position at Biomapas


Date2026-02-19T14:09:00.716Z bot
Biomapas Scientific (Medical) Writing Lead
Experience: 5-years
Pattern: Full-time
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degreePhD
Czechia

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. Role responsibilities: Act as lead for the Scientific Writing team Coach, guide, and support team members Plan and coordinate job tasks, define resources and information required for the execution of the tasks Serve as the primary point of contact for medium - high complexity Scientific Writing projects ​​Act as the lead with respect to content and scientific strategy in complex projects ​Development / review / update of SOPs, Working Instructions, Job Descriptions and etc. ​Write/review/assess a range of scientific documents ​Assess documents for marketing authorisation of medicinal products, clinical studies, other biomedical research to make conclusions and recommendations Contribute to the development of regulatory strategy & clinical research program Participation and contribution in audits ​Contribute to the preparation of financial proposals, service orders, and agreements ​Contribute to the Regulatory Affairs department budget preparation ​Communicate and co-operate with vendors, consultants, and key experts Serve as backup for other team members as required ​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 ​Strong scientific background  ​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

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