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IQVIA

Runs drug trials and sells health data to pharma

Data Team Lead

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeWarsaw, PolandIn-person

About the Job

Requirements

  • A Bachelor's degree in health, clinical, biological, or mathematical sciences, or a related field, with proven experience in Data Management.
  • Three to four years of direct Data Management experience, including at least one year as a CDM project lead.
  • Fluency in spoken English and advanced English proficiency.
  • Advanced proficiency with computer applications such as Microsoft Excel, Word, and Inbox.
  • Advanced understanding of the drug development lifecycle and the overall clinical research process.

Responsibilities

  • Manage end-to-end delivery of data management services for single- or multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget and to customer satisfaction.
  • Provide comprehensive data management expertise to the Data Management team to deliver high-quality products that meet customer needs.
  • Lead the team in project planning, execution, and close-out; oversee financial management for data management activities, communications, and milestone deliverables; and perform the Data Team Lead role.
  • Gather study setup requirements through discussion and communication with relevant stakeholders.
  • Support and oversee validation of new device integrations with minimal guidance.
  • Oversee and perform regular data-cleaning activities to ensure clean data and quality, timely deliverables to the sponsor.
  • Ensure deliverables meet expected quality standards and customer expectations.
  • Ensure, with guidance, that service and quality meet agreed timelines and deliverables in the contract or Scope of Work.
  • Support training of new joiners.
  • Lead internal study meetings and internal or sponsor audits, and participate in study kickoff meetings and other sponsor meetings.
  • Track and manage projects, oversee project progress, identify risks, and take corrective action to rectify errors as needed.
  • Manage and oversee implementation of new technology and database revisions with guidance.
  • Work closely with the programming team on process innovation and automation.
  • Complete required training and read electronic standard operating procedures.
  • Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions.
  • Collaborate in communications with the Line Manager and other cross-functional team members.
  • Perform other duties as directed by the Line Manager.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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