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Location
In office (Beijing, Shanghai)
Seniority
Staff · 3+ years exp
Employment
Full-Time
Overview
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IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

Job Overview

Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).

Essential Functions

  • Gather Study Set up requirements through discussion and communication with relevant stakeholders.
  • With Minimal guidance - support, overview of validation of new Device integrations.
  • Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
  • Ensure that all the deliverables are of expected quality standards and meet customer expectations.
  • With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
  • Support Training of New joiners.
  • Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
  • Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
  • With Guidance manage & oversight the implementation of new technology / database revisions.
  • Work closely with the programming team for process innovation and automation.
  • Be compliant to trainings and eSOP reading.
  • Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
  • Communication with Line Manager, and other team members across functions should be collaborative.
  • Perform other duties as directed by Line Manager.

Qualifications

  • Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req
  • 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref
  • English Fluency Spoken and English Advanced
  • Advanced computer applications like Microsoft excel, word, Inbox etc Advanced
  • Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced

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.

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