Medical Writer

Join our Regulatory Affairs department as a Medical Writer.

Medical Writer is responsible for the preparation and review of various documents used in clinical, nonclinical and epidemiological research and marketing authorization of medicinal products.

Position is in Lithuania, Kaunas.

Role responsibilities:

• Prepare documents for marketing authorization of medicinal products (product information, CTD modules 2-5) and clinical research (study protocols and reports, Investigator’s Brochures, etc.)
• Write manuscripts for scientific journals
• Coordinate package leaflet readability user tests
• Research on topics relevant to assigned projects
• Participation and contribution in audits

Role requirements:

• Master or higher degree in Medicine, Pharmacy, Public Health or Life Sciences
• Fluent written and spoken English
• Previous medical or scientific writing work experience is preferred
• Good understanding of basic human anatomy and physiology
• Familiarity with medical terminology
• Basic knowledge of biostatistics
• Attention to details and analytical skills
• Ability to work independently and within the team

Benefits of being a part of our team:

• Professional growth and career opportunities
• Supportive work environment
• Additional benefits (bonus system, additional health insurance and etc.)
• International team
• Modern and new office in Kaunas with partly remote work possibility


Job Category: Regulatory Affairs
Job Type: Full Time
Job Location: Lithuania
Job Specification: R1

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Allowed Type(s): .pdf, .doc, .docx