Regulatory Submissions Specialist — France

Medpace, Inc. in Lyon is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This role supports the clinical trial management process by preparing and filing regulatory submissions for France and coordinating with study sites to gather required documents.Entry-level positions with permanent contracts are...

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 career where you use your previous expertise and can develop...

Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking a full-timeoffice-basedRegulatory Submissions Coordinator to join our Clinical Operations team inLyon. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

Company DescriptionWith sales of €700m and 3,300 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has...

Company DescriptionWith sales of €700m and 3,300 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has...

DescriptionLocation : Lyon, FranceAbout ARCHIMEDWith offices in Europe, North America and Asia, ARCHIMED is a leading investment firm focused exclusively on healthcare industries. Its mix of operational, medical, scientific and financial expertise allows ARCHIMED to serve as both a strategic and financial partner to healthcare businesses. Prioritized areas...

About The Role The Specialist, Chemical Product Safety Europe is responsible for ensuring the compliance, classification, labelling and safety documentation of chemical products distributed by DKSH across the European Union, the United Kingdom, and Switzerland. Embedded within a 12-person regulatory team, this position plays a critical role in protecting...

Medpace, Inc. is looking for a full-time Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon. This role is crucial for managing the clinical trial process and involves ensuring compliance with regulatory standards.The ideal candidate will have a Bachelor's degree in a Life Sciences field, with at least 4-5 years of relevant...

A consulting firm is seeking a Regulatory Affairs / Clinical Affairs Specialist in Lyon to manage regulatory projects in pharmaceuticals and medical devices. The role involves advising clients on compliance, preparing regulatory submissions, and monitoring changes in regulations. Candidates should have 5-15 years of experience in regulatory affairs, strong...