Senior Clinical Safety Coordinator

Medtronic

Remote
Base: $62,400.00 - $93,600.00; bonus/equity: eligi...
Fully remote
Data coordination and verification
Clinical study document management
Compliance with study protocols
Medtronic is seeking a Senior Clinical Safety Coordinator to support the execution of clinical studies through effective data and document coordination, with a focus on accuracy and compliance. This fully remote position requires candidates to have a strong background in clinical research and data management, alongside a commitment to enhancing healthcare access and equity

Job Summary

  • You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
  • Supports clinical studies by executing and maintaining one or more of the following areas: Data coordination and Document coordination.
  • Medtronic offers a competitive Salary and flexible Benefits Package, including Health, Dental and vision insurance, 401(k) plan plus employer contribution and match, and Paid time off.

Matching Summary

Match Score: 85

Medtronic is seeking a Senior Clinical Safety Coordinator to support the execution of clinical studies through effective data and document coordination, with a focus on accuracy and compliance. This fully remote position requires candidates to have a strong background in clinical research and data management, alongside a commitment to enhancing healthcare access and equity.

Salary

Base: $62,400.00 - $93,600.00; Bonus/Equity: Eligible for Medtronic Incentive Plan (MIP); Benefits: Health, Dental, Vision, HSA, FSA, Life Insurance, LTD, Dependent Daycare FSA, Tuition Assistance, Well-being program, 401(k) match, PTO, Holidays, ESPP, EAP, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan

Skills & Requirements

Must-have

  • Data coordination and verification
  • Clinical study document management
  • Compliance with study protocols
  • Cross-functional team collaboration
  • Proficiency with standard computer applications

Nice-to-have

  • High degree of initiative
  • Advanced practical knowledge of CSC role
  • Ability to train, mentor, or coach
  • Process improvement implementation
  • Experience with SOPs and regulated processes

Key Requirements

  • 6+ years relevant administrative, clinical research, or data coordination experience
  • High school diploma or equivalent
  • Unrestricted U.S. work authorization (for non-Principal level roles)

Work Rights

Unrestricted U.S. work authorization required for non-Principal roles

Sponsorship: available

Tailored Resume

Cover Letter