Associate Site Manager - Oncology - West U.s.

Johnson & Johnson

West U.S., United States
Base: $76,000 to $140,300 depending on location; b...
Fully remote
Bachelor's degree in pharmacy, nursing, or life sciences
Minimum 1 year clinical trial monitoring experience
Valid us driver's license with good driving record
Johnson & Johnson is seeking an Associate Site Manager for Oncology in the West U.S., primarily to act as the liaison between clinical trial sponsors and investigational sites. The role involves ensuring compliance with clinical trial protocols and managing various aspects of clinical trials, including site initiation and monitoring

Job Summary

  • The Associate Site Manager serves as the primary contact between the Sponsor and Investigational Site to ensure inspection readiness through compliance with protocols and Good Clinical Practice.
  • This role involves executing site initiation, monitoring, management, and close-out activities while ensuring accurate data collection and timely resolution of issues found during visits.
  • Johnson & Johnson offers a competitive compensation package including an annual performance bonus, comprehensive health benefits, and eligibility for long-term incentive programs.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Associate Site Manager for Oncology in the West U.S., primarily to act as the liaison between clinical trial sponsors and investigational sites. The role involves ensuring compliance with clinical trial protocols and managing various aspects of clinical trials, including site initiation and monitoring.

Salary

Base: $76,000 to $140,300 depending on location; Bonus: Eligible for annual performance bonus; Benefits: Medical, dental, vision, 401(k), paid time off, parental leave

Skills & Requirements

Must-have

  • Bachelor's degree in Pharmacy, Nursing, or Life Sciences
  • Minimum 1 year clinical trial monitoring experience
  • Valid US Driver's License with good driving record
  • Willingness to travel up to 60% overnight
  • Knowledge of GCPs, SOPs, and local regulations
  • Experience with Phase II and III Clinical Trials preferred

Nice-to-have

  • Oncology therapeutic area experience
  • Process improvement and training contribution
  • Strong written and oral communication skills
  • Analytical risk-based monitoring model implementation
  • Collaboration with cross-functional teams

Key Requirements

  • Bachelor's degree required
  • 1+ years clinical trial monitoring experience
  • Valid US Driver's License required
  • Travel up to 60% required
  • GCP and regulatory knowledge required

Work Rights

Not specified

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