Emploi Regulatory - Toulouse

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators...

We are looking for a home based Clinical Site Lead based in the Paris region. Accountable for building and managing site relationships while overseeing site-level study start-up, conduct, and close-out activities for global programs across different therapeutic Area Act as liaison between the compan...

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in France, particularly in our Lyon office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to conti...

The Clinical Research Associate - L'attaché(e) de recherche clinique position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health...

Description Clinical Trial Manager II in Oncology - Sponsor dedicated - Based in Rueil Malmaison with some Home Based days Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and comm...

CDI Responsable du Contrôle Qualité (F/M/D) Dans le cadre de la mise en place d’une usine de production biotechnologique, Just-Evotec Biologics EU est à la recherche de son responsable du service Contrôle Qualité. Vous rejoindrez une équipe en pleine expansion, multidisciplinaire et collaborative. S...

RF Applications Engineer H/F REF 287 Contract type: Permanent (CDI) Full-time Location: Toulouse or Dublin RHESO.TECH is a recruitment agency specialized in high tech and engineering. Our values: empathy, respect and trust. Company Semi-conductor, international company with RF and IOT portfolio with...

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, techn...

Description Clinical Research Associate II in Oncology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Ou...

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based in Lyon Entry Level Site Payments Analyst to join our Clinical Operations team. This position plays a critical role within Clinical Operations by providing day to day the site payments team...

About deVere Group: deVere Group is one of the world's leading independent financial advisory firms. With a global presence spanning over 100 countries and more than $10 billion under advice, we specialize in providing expert, impartial financial advice and wealth management solutions to our clients...

About the job: The brand sourcer Europe and US is responsible for identifying, evaluating, and securing partnerships with new and existing brands in Europe and in the US that align with Oli’s Lab's strategic goals. The role involves market research, negotiation, and relationship management to ensure...

About us: Our client is a premier regulatory writing consultancy, renowned for its commitment to excellence and innovation in the field. With a focus on empowering a diverse team of experts, the consultancy thrives on fostering an environment where every voice is heard and valued. They are dedicated...

I’m hiring a remote Senior CMC Dossier Manager - you'll lead the charge in crafting the technical eCTD sections essential for ground breaking initiatives. Under minimal supervision, you'll take ownership of coordinating and overseeing the generation of CMC dossiers for both marketing and clinical tr...

BioTalent is headhunting for a French and English speaking (Global) Senior Drug Safety Physician. Responsibilities: Lead clinical safety activities for assigned studies, ensuring compliance with international safety reporting requirements. Provide invaluable medical expertise to our Drug Safety and ...