Principal Clinical Research Scientist

Abbott

Plymouth, Minnesota, United States
Base: $99,300.00 – $198,700.00; bonus/equity: not ...
Clinical trial design and conduct
Scientific data analysis and interpretation
Clinical study protocol development
The Principal Clinical Research Scientist will lead scientific activities for clinical trials in the Electrophysiology medical device division, supporting feasibility, regulatory approvals, reimbursement, and commercial adoption

Job Summary

  • The Principal Clinical Research Scientist will lead scientific activities for clinical trials in the Electrophysiology medical device division, supporting feasibility, regulatory approvals, reimbursement, and commercial adoption.
  • Responsibilities include developing clinical trial designs, writing protocols and reports, analyzing data, and interacting with physician Key Opinion Leaders and cross-functional teams.
  • Abbott offers career development, free medical coverage for employees, an excellent retirement savings plan, tuition reimbursement, and is recognized as a great place to work globally.

Matching Summary

The Principal Clinical Research Scientist will lead scientific activities for clinical trials in the Electrophysiology medical device division, supporting feasibility, regulatory approvals, reimbursement, and commercial adoption.

Salary

Base: $99,300.00 – $198,700.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Clinical trial design and conduct
  • Scientific data analysis and interpretation
  • Clinical study protocol development
  • Medical device regulations and submissions
  • Interaction with Key Opinion Leaders
  • Cross-functional team collaboration

Nice-to-have

  • Innovative and resourceful problem-solving
  • Working in a fast-paced environment
  • Strong attention to detail
  • Mentoring and leadership skills

Key Requirements

  • Advanced degree in science, medicine, or similar
  • 5+ years clinical science experience post-degree
  • Demonstrated scientific writing ability
  • Experience with international medical device regulations
  • Ability to plan and organize complex projects
  • Ability to work with minimal direction

Work Rights

Not specified

Tailored Resume

Cover Letter