Senior Medical Writer: Regulatory Docs

Thermo Fisher Scientific is expanding its Medical Writing FSP team in Europe. Esperienza, qualifiche e soft skill: possiede tutti i requisiti per avere successo in questa opportunità? Lo scopra qui sotto. We seek a Senior Medical Writer to develop high-quality clinical and regulatory documents, ensuring regulatory compliance and company standards....

Thermo Fisher Scientific is expanding its Medical Writing FSP team in Europe. Esperienza, qualifiche e soft skill: possiede tutti i requisiti per avere successo in questa opportunità? Lo scopra qui sotto. We seek a Senior Medical Writer to develop high-quality clinical and regulatory documents, ensuring regulatory compliance and company standards....

Thermo Fisher Scientific sta espandendo il suo team di Medical Writing FSP in Europa. Cerchiamo un Senior Medical Writer per sviluppare documenti clinici e regolatori di alta qualità, assicurando conformità normativa e agli standard aziendali.Il ruolo prevede la redazione e la revisione di documenti, la collaborazione con team multifunzionali e la...

Principal Medical Writer / Sr Principal medical Writer- Sponsor-dedicated Updated: Yesterday Location: Remote, MI, Italy Job ID: -OTHLOC-3531-2DRDescription Principal Medical Writer / Sr Principal medical Writer- Sponsor-dedicatedSyneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the...

Syneos Health, Inc. is seeking a Principal Medical Writer to lead sponsor-dedicated medical writing across studies. You will manage complex deliverables, define document strategy, and coordinate activities with cross-functional teams.The role requires at least 6 years in medical writing, strong knowledge of FDA/ICH guidance, and the ability to mentor junior...

Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Tests, in order to expand the RA Team, is looking for a: Senior Regulatory Affairs Specialist FDA & International Registrations Key Responsibilities Define and implement regulatory strategies to...

Overview As a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape...