Study Operations Lead (R1091661) in London, UK at IQVIA™

Date Posted: 8/12/2019

Job Snapshot

  • Employee Type:
  • Location:
    London, UK
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

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.

Job Summary
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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Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1091661