Medical Writer
Employer · Sanofi
Other health professionalFull-timeTemporaryBudapest
Join our Global Research and Development organization's Vaccines Clinical Documentation subgroup as Medical Writer (MW) and you will be an essential team member to produce high-quality clinical documents (content and format). This is a position for the first level of medical writing with increasing levels of autonomy over time. The incumbent takes responsibility for writing clinical protocols/synopses, core informed consents/assents, clinical study reports, lay summaries and synopsis, and investigator brochures according to Sanofi's standards, international government regulations, and guidelines established by the ICH.
Tasks
- Write clinical documents with increasing autonomy, including Phase I to IV clinical protocols, informed consent forms, clinical study reports, and investigators' brochures
- Ensure a consistent style of presentation of the clinical documents to maintain quality
- Perform data quality checks as required
- Contribute to the production of clinical registration dossiers, including overall EU or US clinical regulatory documentation
- Build and maintain good relationships with clinical personnel, including internal clients and colleagues
- Establish effective cross-functional relationships with local and international counterparts in other departments, especially Regulatory Operations
- Share experience with other medical writers about accommodating special details of clinical studies
Conditions & benefits
International work environmentBring the miracles of science to life alongside a supportive, future-focused team in an international work environment.Flexible workingWork from an Office of the Year 2025 award winner with flexible home office policy.Rewards packageEnjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.Health and wellbeingTake good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.Introduction and trainingAn individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks.Community and eventsJoin a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs).
Requirements
- Experience as a medical writer (or equivalent) demonstrating the ability to write all types of simple documents in English in a clear, precise and concise manner
- Ability to work independently and proactively
- Sense of urgency and respect for deadlines
- Precise and meticulous work, attention to detail
- Strong work ethic, professionalism, organizational skills and ability to follow up
- Ability to work effectively in a multicultural and multilingual environment required
- Technical proficiency in electronic document management and word processing software required, especially Microsoft Word and Excel
- Knowledge / experience on Artificial Intelligence use in documentation and writing activities is advantageous
- Bachelor's degree or equivalent in a field related to science or life sciences
- Native or bilingual English speaker with an excellent command of spoken and written English (fluent level C1)