Clinical Studies Spt Coord Iii

Medtronic UK

Data coordination and management
Clinical study document management
Support clinical studies
Supports clinical studies by executing and maintaining one or more of the following areas: Data coordination and Document coordination

Job Summary

  • Supports clinical studies by executing and maintaining one or more of the following areas: Data coordination and Document coordination.
  • Individual contributors who provide organizational related support or service (administrative or clerical) for other members within the organization.
  • Medtronic offers a competitive Salary and flexible Benefits Package, including eligibility for the Medtronic Incentive Plan (MIP).

Matching Summary

Supports clinical studies by executing and maintaining one or more of the following areas: Data coordination and Document coordination.

Skills & Requirements

Must-have

  • Data coordination and management
  • Clinical study document management
  • Support clinical studies
  • Resolve data discrepancies

Nice-to-have

  • Champion healthcare access and equity
  • Life-long career of exploration and innovation
  • Lead with purpose

Key Requirements

  • Minimum of 4 years of relevant experience
  • Broad practical knowledge of operational systems and practices

Work Rights

Not specified

Tailored Resume

Cover Letter