Praca medical writer

A leading global healthcare company is seeking a Principal Medical Writer in Warsaw. This role is responsible for writing regulatory documents and working closely with clinical and safety teams. Ideal candidates will possess a PhD or equivalent with at least 5 years of clinical regulatory writing experience. The position offers an attractive reward package and opportunities for career growth....

A global medical technology leader in Warsaw is seeking a Medical Writer responsible for preparing Clinical Evaluation Reports and conducting systematic literature searches. The ideal candidate holds a Bachelor’s degree in relevant fields, with 3 to 5 years of experience in medical writing or related areas, preferably in the orthopedic device industry. Proficiency in MS Office and familiarity...

Market Access Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What you will be doing! - Generates compelling dossiers and value communications- dossiers to include...

A leading clinical research organization in Poland seeks a Lead Medical Writer to coordinate and prepare essential documents. Candidates should possess extensive regulatory writing experience, with a strong background in life sciences. You will lead writing projects, ensure alignment with timelines, and guide junior staff. This role offers a unique opportunity to shape the quality of medical...

Principal Medical Writer The Principal Medical Writeris an individual expert contributor capable of independently executing complex writing assignments involving a thorough understanding of clinical trial designs and interpretation of statistically analyzed research data. He/she would be expected to drive and coordinate the process to draft, review and approve written assignments including...

Sr Regulatory Medical Writer - CSR - Remote Home Based Updated: December 3, 2025 Location: Warsaw, MZ, Poland Job ID: -OTHLOC-3553-2DR Description Sr Regulatory Medical Writer - CSR - Remote Home Based Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial...

A leading biopharmaceutical solutions company located in Warsaw, Poland, seeks a Project Data Manager for Medical Writing. This entry-level position will focus on providing technical support for clinical documentation, user training, and tool optimization. Key responsibilities include contributing to tool development initiatives, supporting project teams, and assisting with user onboarding....

Overview About The Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role is an exciting opportunity to contribute to a dynamic, ambitious team in Medical Affairs. You will play a critical part in driving innovation and...

Join to apply for the Technical Writer role at Markforged . Get AI-powered advice on this job and more exclusive features. Markforged (NYSE: MKFG) is leading the digital transformation of manufacturing by revolutionizing how engineers and manufacturers create and innovate. Our unique platform combines software, advanced materials (including cutting‑edge metal and composite technologies), and...

Principal Medical Writer - Regulatory Submission Documents Updated: December 3, 2025 Location: Warsaw, MZ, Poland Job Responsibilities - Lead the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately - Manage medical writing activities associated with individual studies, coordinating these activities within and...

A global clinical research organization in Poland is seeking a Market Access Medical Writer to generate compelling dossiers and manage technical projects. The ideal candidate will have extensive experience in Market Access within the pharmaceutical industry and strong communication skills. You'll be responsible for developing Payer Value Propositions and maintaining client relationships. This...

Site Name: Warsaw, Mississauga Milverton Drive Posted Date: Dec You will be a Principal Medical Writer who turns complex clinical and safety data into clear, regulatory‑ready. You will work closely with clinical, safety, regulatory, statistics and programming colleagues. We value sound scientific judgement, practical problem solving and a collaborative mindset. This role offers growth through...

A global healthcare company in Poland is seeking a Principal Medical Writer to independently execute complex writing assignments. The ideal candidate will have over 7 years of regulatory medical writing experience, especially in oncology, and should demonstrate expertise in managing complex projects. Offering a competitive package with a focus on work-life balance and hybrid working arrangements,...

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support...

Join to apply for the Principal Medical Writer role at GSK Site Name: Warsaw, Mississauga Milverton Drive Posted Date: Sep The Principal Medical Writer is an individual expert contributor capable of independently executing complex writing assignments involving a thorough understanding of clinical trial designs and interpretation of statistically analyzed research data. He/she is expected to...

A biopharmaceutical solutions organization is seeking a Medical Writer Developer to provide technical support for clinical documentation projects. Responsibilities include tool development, user training, and process optimization to enhance documentation workflows. The ideal candidate possesses a relevant degree and experience in technical support for clinical documentation tools. This role is...

A leading biopharmaceutical solutions organization is seeking a Sr Regulatory Medical Writer to lead medical writing deliverables from a remote location. The role requires proven expertise in preparing regulatory documents and mentoring junior writers. Candidates should possess an advanced degree and strong collaborative skills to coordinate writing activities across departments. This position...

A leading global healthcare company is seeking a Principal Medical Writer in Warsaw. The ideal candidate will have extensive experience in clinical regulatory writing, specifically crafting documents for regulatory submissions. Responsibilities include collaborating with cross-functional teams, producing high-quality documentation, and mentoring junior writers. A PhD or equivalent along with 5...

CMC Technical Writer Responsible for incorporating regulatory strategies into regulatory submission documents and ensuring such documents are written and managed to team/project expectations and conform to the regulatory and company standards. Individual may be responsible either for a single product or multiple products. Key Responsibilities - Develop submission plans and contribute to the...

A leading health research organization in Warsaw is seeking a Principal Medical Writer to lead the production of regulatory submission documents. The ideal candidate will have 3-5 years of experience in medical writing within the biopharmaceutical industry and a strong understanding of FDA and ICH regulations. Responsibilities include overseeing the completion of various complex documents and...