Principal Clinical Scientist

AbbVie

Temecula, CA, United States
Base: $99,300.00 – $198,700.00; bonus/equity: not ...
Onsite
Clinical trial design and management
Regulatory submission support
Scientific leadership in clinical studies
Abbott is a global healthcare leader with a diverse portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines, serving people in more than 160 countries

Job Summary

  • Abbott is a global healthcare leader with a diverse portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines, serving people in more than 160 countries.
  • The Principal Clinical Scientist role involves designing clinical trials, providing scientific leadership, supporting regulatory submissions, and collaborating with internal and external stakeholders to advance vascular device products.
  • Employees have access to career development, comprehensive health coverage, retirement savings plans, tuition reimbursement, and a supportive, diverse workplace recognized globally.

Matching Summary

Abbott is a global healthcare leader with a diverse portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines, serving people in more than 160 countries.

Salary

Base: $99,300.00 – $198,700.00; Bonus/Equity: Not specified; Benefits: Health coverage, retirement plans, tuition reimbursement

Skills & Requirements

Must-have

  • Clinical trial design and management
  • Regulatory submission support
  • Scientific leadership in clinical studies
  • Data analysis and interpretation
  • Cross-functional team collaboration
  • Onsite work requirement
  • Experience in quality system environment

Nice-to-have

  • Experience in vascular/cardiovascular fields
  • Publication and presentation strategy development
  • Mentoring junior team members
  • Process and workflow optimization
  • Experience with FDA interactions
  • Knowledge of medical device industry

Key Requirements

  • Bachelor’s Degree or equivalent experience
  • Minimum 8 years related work experience
  • Comprehensive knowledge of clinical research
  • Experience in medical device industry preferred
  • Experience with clinical trials highly desirable
  • Ability to work onsite in specified locations

Work Rights

Not specified

Tailored Resume

Cover Letter