Clinical Studies Spt Coord Ii

Medtronic

Base: not specified; bonus/equity: short-term ince...
Data coordination and management
Clinical study document management
Protocol requirement adherence
Supports clinical studies by executing and maintaining data and document coordination areas, including case report forms, study reports, and study databases

Job Summary

  • Supports clinical studies by executing and maintaining data and document coordination areas, including case report forms, study reports, and study databases.
  • Individual contributors provide organizational support and service, typically under supervision, with established productivity and application of prior experience.
  • Medtronic offers a competitive salary, flexible benefits package, and a commitment to employee well-being, recognizing contributions and sharing in success.

Matching Summary

Supports clinical studies by executing and maintaining data and document coordination areas, including case report forms, study reports, and study databases.

Salary

Base: Not specified; Bonus/Equity: Short-term incentive (MIP); Benefits: Competitive and flexible benefits package

Skills & Requirements

Must-have

  • Data coordination and management
  • Clinical study document management
  • Protocol requirement adherence
  • Data discrepancy resolution

Nice-to-have

  • Life-long career exploration
  • Championing healthcare access
  • Innovative problem solving
  • Collaborative team environment

Key Requirements

  • Minimum of 2 years of relevant experience
  • Full job knowledge of systems and procedures

Work Rights

Not specified

Tailored Resume

Cover Letter