Clinical Trials Assistant

Courbevoie, France | Part time | Field-based | R1520092Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Dijon, France.This role with an immediate start is for 24 hours per week and is expected to last around 7 months.The successful candidate will be...

Due to our continued growth, we are recruiting for a Sr. Clinical Research Associates to join our team. This is a great opportunity for a CRA to join a progressive and developing CRO.IQVIA Biotech is unique division specialising in working with smaller biotech and emerging biopharma clients, and as such we have a vibrant, fast-paced working...

Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies...

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete appropriate therapeutic, protocol and clinical research...

The flex resource performing the Program Delivery Management, IP services will be responsible for the oversight and the training strategy/delivery of Investigational Product (IP) across relevant GCO roles and sites. Activities include engaging with investigational sites as it relates to IP and serving as the internal contact for GCO. The resource will...

IQVIA, fort de ses collaborateurs à travers le monde, est leader dans les informations, les technologies innovantes et les services de recherche clinique dans le secteur de la santé.Issue de la fusion entre IMS Health et Quintiles, IQVIA combine la rigueur analytique, la précision des données et les nouvelles technologies pour répondre aux enjeux des...

**Clinical Trial Manager** Global or Regional Applicability: Regional Trial Management services provide local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned project(s) at the country level for end-to-end project management from...

Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

At IQVIA, we know that meaningful results require not only the right approach but also the right people. Regardless of your role, you’ll have the opportunity to play an important part in helping our clients improve patient healthcare. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across...

The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. Providing administrative support to the clinical teams members could make your contribution to the research. We seek dynamic and motivated people who truly want to...

Courbevoie, France | Part time | Field-based | R1520092 Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Dijon, France. - This role with an immediate start is for **24** **hours**per week and is expected to last around 7 months. - As a pivotal member...

Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...

Job Overview Engage in structured training program to gain knowledge and skills required to independently 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 clinical research...

**Job Overview** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Fluent in French and English.** **Essential Functions** - Oversee the execution of Site Activation...

We are building a new team of Medical Science Liaisons (MSLs) across Europe and are looking for an MSL for France and Belgium. This key field-based role involves establishing and nurturing relationships with Principal Investigators (PIs), Investigators, Key Opinion Leaders (KOLs), and other stakeholders. The MSL will engage in scientific discussions, build...