Freelance Regulatory Affairs Manager

Regulatory Affairs Officer / Linguistic Review Coordinator M/F - 025 EuropeRegulatory AffairsPermanent contractRegulatory Affairs Officer / Linguistic Review Coordinator M/F - 025 To ensure and coordinate the Linguistic Review (LR) for the Centralized products of one of our key clients, we are urgently looking for a Regulatory Affairs Officer / Linguistic...

Regulatory Affairs Specialist 362 In the frame of a project for one of our Top Clients, we are seeking for a Regulatory Affairs Specialist ( pharmacist ) responsible for ensuring the delivery of regulatory activities performed onsite in Paris region. About us Group 10 Responsibilities Under the responsibility of the regulatory coordinator of this...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Regulatory Affairs Project ManagerAbout...

We are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally (internationally).Responsibilities: Prepare and...

Nanobiotix is excited to announce an opening for a CMC Manager, Regulatory Affairs to join their team. In this role, you will play a crucial part in supporting Nanobiotix's mission to advance innovative nanomedicine solutions that have the potential to redefine cancer treatment.Specializing in the development and production of nanoparticles that enhance the...

Summary:Key Responsibilities: Develop, implement, and manage regulatory strategies to ensure compliance with applicable regulations and standards. Monitor changes in relevant regulatory environments, interpret new and existing regulations, and communicate potential impacts to key stakeholders. Provide expert guidance on regulatory matters related to product...

Our pioneering work in the field of synthetic biology has enabled Eligo to be elected as one of the 30 Most Innovative Companies by the World Economic Forum, to receive multiple prestigious international awards. We have also been featured in international media and scientific journals such as Nature Biotechnology, Science, The Economist, The BBC and The New...

Eligo Bioscience mission is to develop treatments and cures for serious diseases in immuno-inflammation, oncology and infectious diseases. Backed by top-tier investors from Silicon Valley and Europe, Eligo is an industry-leading biotechnology company, co-founded by scientists and professors from MIT and the Rockefeller University – now operating in Paris,...

Job Description You join the Global Head of Compliance and Public Affairs team as a regulatory officer. Your mission will be to assist Mirova's challenges, as well as actively contribute to the monitoring of regulatory changes that have an impact on its activities and that of its affiliates located in the USA, In the UK, Kenya and Singapore. In a...

Quelles sont les missions ?Act as the Primary PRRC for Regulatory for the EMEA and LATAM regions: - Lead the Regulatory Affairs Registrations team for approvals and product registrations of all medical devices;- Planning and executing all aspects of Regulatory Affairs and acts as the company's regulatory representative;- Develops, approves, and implements...

Pharmélis, cabinet de recrutement et organisme de formation, spécialiste des postes cadres, d'experts et de dirigeants, partenaire depuis plus de 18 ans des entreprises du secteur Santé (Pharmaceutique, Cosmétique, Dispositifs Médicaux, Biotechnologie), accompagne son client, laboratoire pharmaceutique d'envergure internationale, dans le recrutement...

About FTI ConsultingFTI Consulting combines public policy, capital markets and industry-specific expertise to offer a unique capability for clients operating at the critical intersection between business and government. We are one of the world's most highly regarded communications consultancies with a 30-year track record of serving as trusted advisors...

Freelance Medical Affairs Manager - CNS (Central Nervous System)Location: France (Remote)Committed to improving patient outcomes, we are seeking a talented and experienced Freelance Medical Affairs Manager specializing in CNS to join our dynamic team.As a Freelance Medical Affairs Manager specializing in CNS, you will play a crucial role in driving the...

About FTI ConsultingFTI Consulting combines public policy, capital markets and industry-specific expertise to offer a unique capability for clients operating at the critical intersection between business and government. We are one of the world's most highly regarded communications consultancies with a 30-year track record of serving as trusted advisors to...

Are you an experienced Public Affairs professional with an in-depth knowledge of the French policy arena?Would you like to join a company that is committed to enhancing its impact on the sustainability agenda and becoming a trusted partner among political stakeholders in France?If so, Grundfos is looking for a Senior Public Affairs Advisor to direct its...

The Director, RA CMC Combination Products will work cross-functionally to lead development and implementation of global combination product/Medical Devices regulatory strategies across all applicable programs and lifecycle stages in accordance with program objectives. Advanced degree (eg MS, PhD) preferred. ~ Regulatory CMC experience in medical device and...

Position Summary: ultra focused – Work together to fearlessly uncover new possibilities Working directly with the Responsible Pharmacist & Director of Pharmaceutical Affairs France & Benelux, the Pharmaceutical Affairs Manager / Deputy Responsible Pharmacist, will manage the quality system and ensures compliance with applicable pharmaceutical...

**Notre mission** : aider les professionnels de santé à mieux soigner en apportant la connaissance médicale la plus adaptée pour chaque patient.Posos est **le premier outil d'aide à la décision thérapeutique** capable de croiser instantanément les informations de 170 sources sur les médicaments, pathologies avec les données du patient. Le moteur...

Join our Biopharmaceuticals R&D team as a Regulatory Affairs Manager I, a role that offers the opportunity to contribute to our drug development strategies and turn them into reality. As a regulatory specialist with project management capabilities, you will be responsible for leading the end-to-end planning, coordination, and execution of assigned...

Bausch+Lomb is an innovative company that invests in research to advance health in the world and attaches particular importance to the realization of our commitments to our patients, healthcare professionals, our shareholders and society in general.With 160 years of expertise in this field and a portfolio of products available in more than 100 countries,...