Manager, Regulatory Medical Writing X-TA

Manager, Regulatory Medical Writing X‑TA Apply now About the vacancy Location: Leiden, South Holland, Netherlands. Permanent, full‑time. The position may be located High Wycombe, UK; Leiden, Netherlands; Neuss, Germany; Paris, France; or Beerse, Belgium. The position is Hybrid (3 days onsite weekly). Remote work options may be considered on a...

On-siteOperations, Medical AffairsFull timeEurope, Paris, FranceOVERVIEWDescriptionAbout the JobJoin 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...

About the JobJoin 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 the Medical Writing department. You will play...

A leading healthcare organization in Paris is seeking a Principal Medical Writer to lead the development of high-quality regulatory documents. The ideal candidate will have over 5 years of experience in medical writing for pharma or biotechnology, as well as a Bachelor's degree in a relevant field. Responsibilities include guiding document preparation,...

**About BIORIUS** **About the Position** Historically focused on human health, BIORIUS is adapting to the new constraints and opportunities suggested by its market. The Medical Device business unit recruits a Regulatory Affairs / Quality Specialist. Since many developments are expected and capacity building is needed, this position requires a senior...

Cerner Enviza an Oracle company is a leading global healthcare consulting firm and trusted advisor to many of the world’s top pharmaceutical, biotech, and medical device & diagnostic companies. By supporting the work of Cerner Enviza, you will work with world-class healthcare companies, helping them improve global access to medicines by connecting science...

A global healthcare research organization seeks a Senior Medical Writer to enhance clinical research documentation. This role involves developing high-quality documents such as Clinical Study Reports and protocols while ensuring compliance with regulatory standards. Candidates should have an advanced degree in Life Sciences, alongside 3-5 years of medical...

Prise de poste non définie BAC +5 Paris Nombre de postes non défini CDI Rémunération non définie **Description du poste et des missions**: **WHO WE ARE** Cellectis is a **global clinical-stage biopharmaceutical** company. **Pioneers and innovators** in our field, our mission is to develop **innovative treatments** for **patients with unmet medical...

A fast-growing global AI company is seeking an experienced Medical Writer with a background in pharmacovigilance to join their innovative team. This hands-on role focuses on leveraging AI and automation to streamline regulatory document creation while maintaining the highest quality standards. Key Responsibilities Develop and maintain templates and content...

Principal 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. We are currently seeking Senior or Principal Medical Writer to join our...