Associate Clinical Lead - WHC165

Associate Clinical Lead - WHC165

16 nov
Iqvia Argentina
Buenos Aires C.F.

16 nov

Iqvia Argentina

Buenos Aires C.F.

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healthier world. Start right here at IQVIA.

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

The Study Operations Lead is the main point of contact for the sponsor and manages the client relationship, oversees payment management projects and ensures sponsor satisfaction is achieved.

The Study Operations Lead manages and oversees the initiation and study management of protocols including identifying all protocol related information, timelines, reporting and initial setup of proprietary software system used to initiate studies.

Summary of Essential Job Functions

Acts as the primary point of contact for assigned sponsor(s) and associated studies

Responsible for managing the project timeline and identify/pursue change orders and coordinating with the contracts management team

Prepares materials and KPi’s for sponsor governance meetings and participates as appropriate

Identify and execute process improvement initiatives when appropriate

Prepares, arranges and executes regular client meetings and ensures all necessary materials are prepared with accuracy and completeness

Function as the engagement leader providing management throughout the length of the clinical trial by overseeing activities of the project team to ensure sponsor commitments and DrugDev’ service levels are achieved.

Coordinates with Site Operations and Data Operations to ensure proper resource assignment and service delivery quality

Ensure that DrugDev financial interests are appropriately protected through diligent scope of work management efforts

Ensure support to the clinical trial sites is provided at DrugDev’ levels of excellence through timely resolution of issues that are raised through email and/or phone contact

Responsible for ensuring that payments do not exceed SOW timelines

Responsible for ensuring change orders are executed and communicated to appropriate personnel

Responsible for performance review input to Site Operations and Data Operations for roles that support assigned sponsor

Coordinates with the Site Operations team members to prepare sponsor funding

Ensure that all DrugDev processes and standards are followed and that appropriate financial controls are observed and are in line with sponsor requirements for managing and mitigating financial risk

Ensures work is SSAE 16 compliant were appropriate

Responsible for monitoring, assist in resolving and escalating operational and performance metric issues

Other duties as assigned

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