Senior Clinical Project Specialist

Abbott

Maple Grove, Minnesota, United States
Base: $78,000.00 – $156,000.00; bonus/equity: not ...
Clinical device studies execution
Compliance to study protocol
Good clinical practices
Participate in the execution of Abbott clinical device studies, ensuring compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards, and Abbott Standard Operating Procedures

Job Summary

  • Participate in the execution of Abbott clinical device studies, ensuring compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards, and Abbott Standard Operating Procedures.
  • Manage all aspects of subject selection committee work, including tracking and results-oriented communication of data entry needs/timelines, and facilitating timely committee member adjudications.
  • Abbott offers career development with an international company, access to a Health Investment Plan (HIP) PPO medical plan, an excellent retirement savings plan, tuition reimbursement, and is recognized as a great place to work globally.

Matching Summary

Participate in the execution of Abbott clinical device studies, ensuring compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards, and Abbott Standard Operating Procedures.

Salary

Base: $78,000.00 – $156,000.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Clinical device studies execution
  • Compliance to study protocol
  • Good Clinical Practices
  • Vendor oversight
  • Subject selection committee work
  • Data entry tracking and communication

Nice-to-have

  • Career development opportunities
  • Work-life balance
  • Company recognized as great place to work
  • Familiarity with cardiac technologies

Key Requirements

  • Associate's Degree (± 13 years)
  • Minimum 7 years related experience
  • Bachelor's degree in natural science, pre-medicine, nursing, bioengineering, or related field
  • Minimum 3 years in clinical operations or healthcare related field
  • Demonstrated strong communication and organizational skills
  • Proficiency in Microsoft Office Suite
  • Certification as a Research Professional (SoCRA or ACRP)

Work Rights

Not specified

Tailored Resume

Cover Letter