Associate Clinical Data Manager

2 weeks ago

Sydney, New South Wales, Australia IQVIA Full time

Responsibilities:

  • Gather Study Set up requirements through discussion and communication with relevant stakeholders.
  • Perform Database Set up and validation to ensure quality study design for data collection.
  • Support validation of new Device integrations.
  • 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.
  • 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 by DTL.
  • Manage the development and 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, Leadership and other team members across functions should be collaborative.

Skills and experience required:

  • Bachelor's degree or educational equivalence in clinical, biological or mathematical sciences or related field OR a nursing qualification or equivalent combination of education, training and experience.
  • Robust understanding of medical terminology and jargon required.
  • At least 3 years of relevant experience in clinical data management.
  • Strong EDC experience in clinical trials coupled with DM queries (familiarity with EDC platforms).
  • SAS experience is not required, although good to have (database design).

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