Senior Clinical Trial Specialist

Johnson & Johnson Innovative Medicine

Cincinnati, Ohio, United States of America
Base: $109,000.00 - $174,800.00; benefits: eligibl...
Clinical trial protocol compliance
Good clinical practices (gcps)
Site monitoring activities
This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization

Job Summary

  • This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization.
  • The Senior Clinical Trial Specialist ensures inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and applicable regulations and guidelines from study start-up through clinical study report.
  • The anticipated base pay range for this position is : $109,000.00 - $174,800.00.

Matching Summary

This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization.

Salary

Base: $109,000.00 - $174,800.00; Benefits: Eligible for Company's consolidated retirement plan (pension) and savings plan (401(k)), long-term incentive program, vacation, sick time, holiday pay, work/personal/family time, parental leave, bereavement leave, caregiver leave, volunteer leave, military spouse time-off; Bonus/Equity: Not specified

Skills & Requirements

Must-have

  • Clinical trial protocol compliance
  • Good Clinical Practices (GCPs)
  • Site monitoring activities
  • Clinical trial document development
  • Investigational device management
  • Adverse Event reporting

Nice-to-have

  • Cross-functional collaboration
  • Global evidence generation strategies
  • Problem-solving during study execution
  • Digital literacy in clinical systems

Key Requirements

  • Minimum of a Bachelor’s degree
  • Minimum of 4 years of professional work experience
  • Previous clinical research experience
  • Previous medical device site monitoring experience
  • Understanding of clinical research regulations
  • Proficient in speaking and writing English

Work Rights

Not specified

Tailored Resume

Cover Letter