Clinical Project Coordinator

MEDTRONIC

Competitive salary; short-term incentive (mip); fl...
4 years clinical study experience
Ctms and etmf system proficiency
Study dossier preparation skills
The role involves supporting clinical studies by executing startup, maintenance, and close-out activities including study dossier preparation and site binder dispatch

Job Summary

  • The role involves supporting clinical studies by executing startup, maintenance, and close-out activities including study dossier preparation and site binder dispatch.
  • Candidates must possess strong attention to detail to ensure data quality, resolve discrepancies, and support audits for accuracy and compliance.
  • Medtronic offers a competitive salary, flexible benefits package, and eligibility for the Medtronic Incentive Plan (MIP) to support employee success.

Matching Summary

The role involves supporting clinical studies by executing startup, maintenance, and close-out activities including study dossier preparation and site binder dispatch.

Salary

Competitive Salary; Short-term incentive (MIP); Flexible Benefits Package

Skills & Requirements

Must-have

  • 4 years clinical study experience
  • CTMS and eTMF system proficiency
  • Study dossier preparation skills
  • Data quality and audit support
  • Investigational product logistics

Nice-to-have

  • Strong written communication skills
  • Proactive team player mindset
  • Ability to manage multiple tasks
  • Fast-paced environment adaptability

Key Requirements

  • Minimum 4 years relevant experience in clinical studies
  • Hands-on involvement in data coordination
  • Experience with clinical documentation management

Work Rights

Not specified

Tailored Resume

Cover Letter