Responsibilities include, but are not limited to: • Trial and site administration: o Track (e.g. essential documents) and report o Ensure collation and distribution of study tools and documents • Document management: o Prepare documents and correspondence o Collate, distribute/ship, and archive clinical documents, e.g. eTMF o Assist with eTMF reconciliation o Execute eTMF Quality Control Plan • Site Start-Up responsibilities: Collaborate with other country roles to: o In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions o Obtain, track and update study insurance certificates • Budgeting, Agreement and Payments: Collaborate with finance/budgeting representatives for: o Develop, control, update and close-out country and site budgets (including Split site budget) o Develop, negotiate, approve and maintain contracts (e.g. CTRAs) o Track and report contract negotiations o Update and maintain contract templates (in cooperation with Legal Department) o Calculate and execute payments (to investigators, vendors, grants) o Ensure adherence to financial and compliance procedures o Monitor and track adherence and disclosures o Maintain tracking tools • S/AE Claim Management: Support Financial Clinical Operation Manager(F-COM) for: o Coordinate meetings o Update and maintain tracking tools o Develop and maintain settle agreements o Coordinate for payments o Collate, distribute/ship, and archive relevant documents IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

Clinical Trial Coordinator.

more at Iqvia.

Senior Clinical Data Analytics & Reporting Programmer

Clinical Trial Assistant

Associate Consultant - Onsite Deployment Unit

similar roles.

Disponent im Zugverkehr (m/w/d)

Disponent im Bahnbetrieb (m/w/d)

Agent(e) d’admission en santé mentale (nuit)

Shuttle Driver - The Wren

Owner Services Manager - The Residences Bachelor Gulch

Line Cook - Marlin Moon