Regulatory & Start-Up Specialist – Site Activation (France)

A leading clinical research provider is seeking a Regulatory & Start-Up Specialist to manage site activation tasks in France. The role entails ensuring compliance with regulations and facilitating regulatory submissions. Preferred candidates will have a B.Sc. in Life Sciences and 1-3 years of clinical research experience. Fluency in French is essential for...

Regulatory & Start Up Specialist, IQVIA Biotech, France page is loaded## Regulatory & Start Up Specialist, IQVIA Biotech, Francelocations: Paris, Francetime type: Full timeposted on: Posted Todayjob requisition id: R1515222**Regulatory & Start-Up Specialist 1****IQVIA Biotech****France****Homebased**IQVIA Biotech partners exclusively with biotech and...

Regulatory & Start-Up Specialist 1 IQVIA Biotech France Homebased IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative...

Regulatory & Start-Up Specialist 1IQVIA BiotechFranceHomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative...

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific...

IQVIA MedTech Clinical Solutions, specializes in clinical research for Medical Devices and In-Vitro Diagnostic (IVD) products.- IQVIA MedTech’s focused expertise meets the growing needs of device Sponsors to justify product safety and effectiveness as well as reimbursement and adoption challenges due to increased scrutiny by regulators, end-users, and...

Job Overview Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

Nous recrutons sur Paris un Study Start Up Specialist H/F. Vous aurez pour principales missions: - Préparation et relecture des documents d’études (synopsis, brochure investigateur ) - Soumissions réglementaires des demandes d’autorisation d’essai clinique et amendements - Etude de faisabilité et mise en place des études cliniques - Formation...

Vous serez en charge de la responsabilité d’un portefeuille de start-Up ainsi que du fonctionnement du programme d’accélération de start-Ip, Gene.io au sein du département Emergence et sous la responsabilité de son Directeur. **Vos principales missions seront les suivantes**: 1. Responsabilité d’un portefeuille de start-Up en phase...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service,...