Senior Clinical Trial Specialist

Johnson & Johnson

Cincinnati, Ohio, United States of America
Base: $109,000.00 - $174,800.00; bonus/equity: not...
Clinical trial protocol compliance
Good clinical practices (gcps)
Site monitoring activities
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

Job Summary

  • 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.
  • This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization.
  • The anticipated base pay range for this position is : $109,000.00 - $174,800.00.

Matching Summary

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.

Salary

Base: $109,000.00 - $174,800.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours for an immediate family member, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours per calendar year, Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Must-have

  • clinical trial protocol compliance
  • Good Clinical Practices (GCPs)
  • site monitoring activities
  • clinical trial documents development
  • Adverse Events (AE) reporting

Nice-to-have

  • innovative healthcare solutions
  • inclusive work environment
  • cross-functional collaboration
  • global evidence generation strategies

Key Requirements

  • Bachelor's degree or equivalent
  • 4+ years professional work experience
  • Previous clinical research experience
  • Medical device site monitoring experience
  • Proficient in English speaking and writing

Work Rights

Not specified

Tailored Resume

Cover Letter