Regulatory Submissions Lead — Paris Hybrid

Ipsen is seeking a Senior Manager and lead programmer to drive multiple studies within the Statistical Programming function, ensuring quality and on-time delivery, either in-house or via CROs.The role requires hands-on and managerial expertise, with strong SAS skills, CDISC knowledge, and experience in SDTM/ADaM programming for regulatory submissions....

Natixis Investment Managers International (Natixis IMI) in Paris seeks a Legal Product Operations & Coordination Manager to oversee the legal life of products, launches, marketing, and compliance within a global asset management group.In an international, hybrid environment, you will coordinate with affiliates and internal clients, manage cross-functional...

Confidential Search in the Paris Region is seeking a Head of Regulatory CMC - Small Molecules to lead the global CMC regulatory strategy for a portfolio spanning small molecules, ASO and ADC assets, from early through late-stage development.Reporting to the Global Head of Regulatory CMC, this newly created leadership role offers autonomy from day one and a...

Finary SAS is seeking an Operations leader who will drive wealth-technology systems in Paris with hybrid work. You’ll build the operating framework that scales wealth aggregation and investment services, while ensuring regulatory alignment and excellent client experience.You will lead a small team, ship internal automation tools, and use AI to multiply...

OverviewTitle: Senior Consultant – Device Regulatory Documentation & ComplianceLocation: Paris (3 days onsite - 2 WFH)The CompanyWe believe great work happens when brilliant minds come together with a shared purpose. This biopharma company is known for its dedication to employee happiness, its collaborative environment, and its passion for bringing...

ICON is seeking a Senior Clinical Research Associate in Paris or Lyon with hybrid or remote options. You will monitor Phase I-III trials, qualify and initiate sites, manage regulatory submissions, and ensure data integrity and patient safety across diverse therapeutic areas.The role requires an advanced degree in life sciences or related fields, proven CRA...

Head of Regulatory CMC - Small Molecules, Paris Region | Hybrid | Confidential Search A global pharmaceutical group with an ambitious, fast-growing development pipeline is seeking a Head of Regulatory CMC - Small Molecules, to lead the global CMC regulatory strategy for a portfolio spanning small molecule, oligonucleotide (ASO) and antibody-drug conjugate...

We are looking for a hands-on and strategic Regulatory Affairs & Quality Assurance Specialist to help bring our technology from development to global commercialization. You will join our Compliance department (Quality Assurance, Regulatory Affairs & Clinical Affairs) and report to the Head of Compliance. You will work at the intersection of innovation,...

Principal Consultant, Medical Devices Regulatory & QualityParis-Hybrid--Medical Device and MedTech Services-Permanent contractWe are looking for a Principal Consultant in Medical Devices Regulatory Affairs and Quality to join our team in Paris. You will lead international regulatory and quality projects, advise clients on market-access strategies, and...