Director, Cross Ta Clinical Risk Mgmt

Johnson & Johnson MedTech

Raritan, New Jersey, United States of America
Base: $150,000.00 - $258,750.00; bonus/equity: not...
Fully remote
Gcp quality and clinical trials experience
Risk-based trial oversight
Quality risk management
Johnson & Johnson MedTech is seeking a Director of Cross TA Clinical Risk Management to oversee risk management in clinical trials for various therapeutic areas. The ideal candidate will have extensive experience in the healthcare industry, strong leadership skills, and a deep understanding of clinical quality assurance

Job Summary

  • Oversee the execution of data-driven, risk-based trial and program oversight activities that deliver quality in the execution of clinical trial programs, compliance with regulatory requirements and internal procedures, and that there is a continued state of inspection readiness.
  • Manage a team of CRM representatives that will provide consistent quality oversight to clinical trials in the Cross TA portfolio.
  • The Director, Cross TA Clinical Risk Management is highly visible to the RDQ Leadership team and ensures robust quality trial oversight of the Cross TA portfolio through quality risk management and execution of quality support services.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Director of Cross TA Clinical Risk Management to oversee risk management in clinical trials for various therapeutic areas. The ideal candidate will have extensive experience in the healthcare industry, strong leadership skills, and a deep understanding of clinical quality assurance.

Salary

Base: $150,000.00 - $258,750.00; Bonus/Equity: Not specified; 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

Skills & Requirements

Must-have

  • GCP Quality and clinical trials experience
  • Risk-based trial oversight
  • Quality risk management
  • Cross-functional team collaboration
  • Strategic communication framework

Nice-to-have

  • Data analytics and visualization tools
  • Data Science and Digital Health
  • Health Authority Inspection experience
  • Immunology Drug Development experience
  • Inclusive leadership

Key Requirements

  • Bachelor’s degree in scientific, medical, or related discipline
  • 10+ years in healthcare industry
  • People leadership experience
  • Proficiency in Microsoft Office Applications
  • English speaking and writing proficiency

Work Rights

Not specified

Tailored Resume

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