Regulatory Submissions Jobs in France

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory s...

Are you ready to make an impact in global regulatory affairs Were seeking talented professionals with at least 2 years of experience in EU/EMA or US-FDA submissions (Pharma/Biologics) to join a long-term project supporting regulatory lifecycle management for human medicinal products.As a Regulatory...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

The CMC Technical Project Manager provides day-to-day operational management for CMC development and technical transfer projects. Working in close partnership with the CMC Technical Senior Project Manager who leads project management activities the CMC Technical Project Manager leverages their techn...

At IQVIA Biotech we partner with visionary biotech companies to transform innovation into patent impact. With dedicated teams deep therapeutic expertise and a biotech tailored model we accelerate clinical development from early phase through global registrational studies. The successful candidate mu...

Who we are Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.Its portfolio includes several medical franchises and international brands including...

Title:Senior Manager Biomarker OperationsCompany:Ipsen Innovation (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experienc...

Shape the future of regulatory excellence at IQVIAAt IQVIA we work to advance healthcare by helping our clients bring safe effective medicines to patients. As a Regulatory Affairs Manager you will play a key role in ensuring compliance and supporting successful product lifecycle management in France...

Shape the future of regulatory excellence at IQVIAAt IQVIA we work to advance healthcare by helping our clients bring safe effective medicines to patients. As a Regulatory Affairs Manager you will play a key role in ensuring compliance and supporting successful product lifecycle management in France...

Do you want a job with a purpose And do you want to make healthcare safer better and more reliableJoin our Team!Join us as our Pre Market Quality and Regulatory Specialist at Dedalus one of the Worlds leading healthcare technology companies in France in Bordeaux to do the best work of your career an...

At Nemera we are passionate about developing innovative drug delivery solutions that truly make a difference in patients lives. To support our continued growth we are currently looking for passionate people ready to make a difference in the following open position: Post market surveillance (PMS) and...

As a Principal Medical Writer you will provide communication expertise and lead a strategy-driven approach to authoring of key clinical and regulatory documents and regulatory submissions to ensure clarity credibility and consistency of clinical information throughout submission packages and clinica...

Your RoleIn a few words: You will contribute to the scientific and operational execution of Resiliences clinical studies supporting the delivery of key trials including sponsored studies and upcoming Life Sciences partnerships with rigor speed and compliance. You will work across multiple studies...

DescriptionOracle Life Sciences empowers pharmaceutical biotechnology medical device companies and clinical research organizations to bring therapies to market faster and more efficiently. We are helping organizations accelerate innovation and improve health outcomes for patients worldwide.With ongo...

Title:Senior Manager CMC RegulatoryCompany:Ipsen Innovation (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with...

Title:Post Doctorant Immuno-OncologyCompany:Ipsen Innovation (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience wit...

Title:Principal Scientist - ImmunogenicityCompany:Ipsen Innovation (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experien...

Title:Head of Bioanalysis Immunoanalysis and OneLabCompany:Ipsen Innovation (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development...