Emplois IQVIA en France

External Job Description · Job Overview · Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. · Essential Functions · Complete appropriate therapeutic, protocol and cl ...

IQVIA is expanding its team and is now seeking an additional Senior Medical Science Liaison (MSL) based in South of France. This is one of several newly created roles across the EU due to our customer's ongoing success, and ahead of product launches in 2026.  · Our customer is a ...

We are seeking a Scientific Report Writer to support full Clinical Study Report (CSR) writing for Phase 1 , protocol development, · and preparation of regulatory modules (2.7.1/ This role requires strong scientific writing skills and attention to detail · to ensure high-quality, ...

Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. · ...

Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their enti ...

Contribuir a mejorar el acceso a los tratamientos innovantes como Délégué(e) Hospitalier para las regiones Bretagne - Pays de la Loire. · Pilotar actividades comerciales y desarrollar relaciones estratégicas con actores hospitalarios y especialistas. · ...

++Vous souhaitez contribuer à améliorer l'accès des patients aux traitements innovants ? Rejoignez-nous en tant que Délégué(e) Hospitalier pour les régions Normandie - Hauts de France. · +Expérience confirmée dans la vente de produits pharmaceutiques, notamment auprès des pharmac ...

Negociar con distribuidores farmacéuticos para asegurar disponibilidad de productos. · ...

Nous participons à la mise en place d'un système de santé plus moderne et efficace. · ...

A global clinical research provider is seeking a Senior Psychometrician responsible for managing complex projects focused on psychometric evaluations of Clinical Outcome Assessment instruments in clinical trials. The ideal candidate will hold a Master's or PhD with extensive expe ...

Location · Uk, France, Netherlands, Spain, Greece & Portugal · Work Model · Hybrid or Office based · The Role · The Senior Psychometrician will be responsible for the on‑time completion and the scientific soundness of projects or components of large, complex projects focusing on ...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials. Joining the team provides the opportunity to manage wide span of phases of clinical research projects in var ...

Courbevoie, France | Full time | Home-based | R1518971 IQVIA is a global leader in healthcare intelligence committed to defining and delivering the future of healthcare. · Lead mentor and develop regulatory publishing staff in line with IQVIAs values and policies · Oversee creati ...

Vous souhaitez contribuer à améliorer l'accès des patients aux traitements innovants ? Rejoignez-nous en tant que Délégué(e) Hospitalier pour les régions Centre Val de Loire / Bourgogne Franche Comté. · ...

A la croisée de deux univers, la santé et les nouvelles technologies, IQVIA est l'expert des données de santé depuis plus de 60 ans et dans 140 pays. Nous participons à la mise en place d'un système de santé plus moderne, plus efficace et plus adapté aux besoins de chacun. · ...

We are recruiting for a Sr. Clinical Research Associates to join our team. · ...

Clinical Trial Educators collaborate with research staff to drive trial recruitment and support study-specific training needs. · Works with research sites to develop study-specific action plansProvides education to healthcare professionals on study protocols ...

We are seeking a Market Access and Public Affairs Manager based in France to contribute to the market access strategy in a company which operates in diverse, highly specialist therapy areas. This is a fantastic opportunity to drive commercial success for biosimilars in the retail ...

Plan and conduct independent audits to assess compliance with regulations, guidelines and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff management and customers. · ...

The flex resource performing the Program Delivery Management services will be responsible for the oversight and training strategy/delivery of Investigational Product across relevant GCO roles and sites. · ...