Regulatory Submissions - 25+ offres

Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon . This position plays a key role in the clinical trial management process at Medpace. If you want

Medpace, Inc.

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting c

Biotech Health Data Governance Lead (AI Training) About The Role What if your expertise in biotech data governance could directly shape how AI understands and works with clinical and research data — at the frontier of life sciences and artificial intelligence? We're looking for a Biotech Health Data

Medpace

A leading clinical research organization in Lyon is seeking a full-time Regulatory Submissions Coordinator to join their Clinical Operations team. This position is crucial for managing clinical trial submissions in compliance with regulations. The ideal candidate will possess a Bachelor's degree in

Sanofi

Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail. This job offer is accessible to all, regardless of gender. Job title: Senior Capability Analyst Location: Gentilly/FR -Marcy l'Etoile/FR A

elemed

A biopharma company in Paris is seeking a Senior Consultant for Device Regulatory Documentation & Compliance. In this role, you will mentor a team, develop regulatory documentation, and ensure compliance for medical devices and combination products. This opportunity is perfect for someone with 5–7 y

Balt

A leading medical device company in Île-de-France is seeking an EMEA International Registration Manager. This role involves managing product registrations, ensuring compliance with regulations, and supporting the development of medical devices. The ideal candidate should have 4-5 years of experience

Servier Group

A leading pharmaceutical company is seeking a Senior Medical Writing Project Lead located in Saclay, France. This role involves leading the development of high-quality English-language medical writing deliverables, managing cross-functional teams, and mentoring junior writers. The ideal candidate wi

Sobi - Swedish Orphan Biovitrum AB (publ)

A global biopharmaceutical company is seeking a Principal Medical Writer based in Paris. The role involves leading the authoring of key clinical and regulatory documents to support submissions, coordinating cross-functional writing teams, and ensuring compliance with regulatory standards. Ideal cand

ICON Strategic Solutions

A leading clinical research organization is seeking a Study Start Up Associate II to join their team in the Paris area. This pivotal role involves leading the initiation of clinical trials and ensuring regulatory compliance. Candidates should have a Bachelor's degree in life sciences and at least 2

IQVIA

A global healthcare provider is seeking a Regulatory Affairs Manager in Paris. In this role, you will ensure compliance for medicinal products and manage regulatory submissions. Candidates should have a Bachelor's in Pharmacy or Life Sciences, with at least 3 years of experience in EU regulatory aff

Crossing Hurdles

A leading regulatory consultancy seeks a Regulatory Medical Writer to work remotely and contribute to FDA submissions. The ideal candidate will have proven experience in preparing regulatory documents for pharmaceuticals or biotechnology. Responsibilities include developing prompts for submissions,

Parexel

A prominent regulatory consultancy is seeking a Senior Regulatory Affairs Associate to serve as the France Local Regulatory Responsible (LRR). This role involves developing regulatory strategies and ensuring compliance with French and EU regulations. The ideal candidate should have at least 5 years

elemed

A healthcare technology firm is seeking a Senior Regulatory Affairs Consultant to develop and execute regulatory strategies compliant with global requirements. The role requires leading FDA submissions and managing design controls. Ideal candidates should have 5-7 years of experience in regulatory a

MSD France

Job Description Dans notre entreprise, nous vous encourageons à inventer pour la vie. Vous rejoindrez une équipe diversifiée, inclusive, où le patient est au centre de toutes nos actions. En effectuant votre alternance dans notre entreprise, vous aurez l'opportunité de vous développer au sein de l'u

Laboratoires Pierre Fabre

We are seeking a Population PK/Pharmacometrics Modeler to join the Pharmacokinetics and Toxicology team within the Pierre Fabre R&D Pharma in Toulouse to support oncology programs (Langlade site, Oncopole). Who You are You are a proactive pharmacometrician who translates clinical trial data into str

ICON Strategic Solutions

Regulatory Submissions Manager (EU CTR) 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.

Universal Medica Group

Date de début : Dès que possible Lieu de travail : SAINT CLOUD (92) - TOULOUSE (31) - BORDEAUX (33) - TOURS (37) Durée : CDI Depuis 2001, Universal Medica Group s’est imposé en France et en Europe pour devenir un partenaire privilégié des acteurs de santé, nous avons pour mission d’apporter conseils

Job Description Join our team as a Senior Biostatistician specialized in oncology and become a key contributor to the analysis, interpretation, and quality control of critical clinical data supporting regulatory submissions and scientific publications. 🔥 Your Responsibilities: Analyze clinical and

Sanofi

Intitulé du poste: alternance 12 mois - affaires réglementaires globales vaccins Lieu : Marcy l’Etoile A partir de : septembre 2026 À propos du poste En tant qu’alternant.e au sein de notre service Affaires Réglementaires Globales Vaccins Franchise Grippe, vous allez apporter votre support à l’équip