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IQVIA

Runs drug trials and sells health data to pharma

Data Acquisition Expert - EDC

Clinical Research OperationsUpdated on Nov 12
Full-timeNo salary listed

About the Job

Requirements

  • A minimum of 5 years of experience building electronic data capture databases in support of clinical research.
  • Technical experience building electronic data capture systems in Medidata Rave, including complex database builds.
  • Demonstrated project management skills.
  • Advanced knowledge of custom functions programming.
  • Experience working on clinical trials.
  • Experience working in highly diverse, cross-functional, global, and multiregional teams within clinical research.
  • Working knowledge of Good Clinical Practice and International Council for Harmonisation guidelines.
  • Knowledge of Clinical Data Acquisition Standards Harmonization.

Responsibilities

  • Assess electronic data capture collection requirements per protocol and create study start-up electronic case report form packages based on global electronic case report form libraries.
  • Design electronic case report form layouts, including form dynamics.
  • Program edit checks and custom functions.
  • Create and configure technical specifications for trial-specific source data verification, Safety Gateway integration, and data mart mappings.
  • Implement electronic data capture coding configurations based on trial-defined coding requirements.
  • Perform test and production Medidata Rave electronic data capture migrations.
  • Oversee planning, requirements, and implementation of Interactive Web Response System integrations to electronic data capture.
  • Serve as a subject matter expert for complex elements of electronic data capture database builds, including integrations and optimal custom function implementation.
  • Provide junior staff with training on electronic data capture build and migration processes and tools.
  • Participate in process, system, and tool improvement initiatives within clinical data management.

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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