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About QFR IQVIA RDS France
Solutions to help life sciences organizations drive healthcare forward and get the right treatments to patients, faster.
9 Job openings in Qfr Iqvia Rds France
Associate Translations Manager eCOALocation: Spain Home basedJob OverviewThe Associate eCOA Translation Manager will join a collaborative and dedicated global team that provides quality eCOA services to our clients. Our team works cross-functionally with internal stakeholders translat More...
Essential Functions Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors studies as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SSAE16 Controls Responsible to accurately comple More...
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 Functions More...
Job OverviewManage 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. Support senior leadership on resourcing strategies and with local clients relationship.Essential More...
Job OverviewDelivers study set up data integration system configuration and testing within sample tracking software systems. interfacing with internal and external stakeholders. Trains and assists end users with system usage. Gather requirements from end users and designs and implemen More...
CRA Internship Office Based ParisIQVIA Offers fantastic opportunity for students who wish to become a CRA.By joining IQVIA as CRA Intern you will engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accorda More...
Job OverviewDirect and manage an assigned team of epidemiology staff who provide epidemiology leadership to sponsored research programs to ensure quality time and budget deliverables are met with a focus on inregion staff and structure (US EMEA APAC).Work closely with global clients a More...
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 Functions More...
MAIN RESPONSIBILITIES Availability on a 24/7 basis to receive calls from the local Competent Authority as required. Act as the contact point for Pharmacovigilance inspections. Respond to requests from Competent Authorities to evaluate the benefits and risks of a medicinal product to i More...