Senior Site Manager - Oncology

Johnson & Johnson

Raritan, New Jersey, United States of America
Base: $92,000 to $148,350 (other us locations); bo...
Fully remote
2 years clinical trial monitoring experience
2 years oncology therapeutic area experience
Good clinical practice (gcp) knowledge
Johnson & Johnson is seeking a Senior Site Manager in Oncology for its Innovative Medicine R&D division, a fully remote position available across the United States. The role involves managing clinical trial sites, ensuring compliance with protocols and regulations, and collaborating with trial teams to drive successful outcomes

Job Summary

  • The Senior Site Manager serves as the primary contact between the Sponsor and Investigational Site to ensure inspection readiness through compliance with GCP and company SOPs.
  • This role involves executing site initiation, remote and on-site monitoring, and close-out activities while implementing risk-based monitoring models at the site level.
  • Johnson & Johnson offers a competitive compensation package including an annual performance bonus, long-term incentives, and comprehensive benefits such as medical, dental, vision, and parental leave.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Site Manager in Oncology for its Innovative Medicine R&D division, a fully remote position available across the United States. The role involves managing clinical trial sites, ensuring compliance with protocols and regulations, and collaborating with trial teams to drive successful outcomes.

Salary

Base: $92,000 to $148,350 (other US locations); Bonus: Annual performance bonus eligible; Benefits: Medical, dental, vision, life insurance, 401(k), and paid time off

Skills & Requirements

Must-have

  • 2 years clinical trial monitoring experience
  • 2 years Oncology therapeutic area experience
  • Good Clinical Practice (GCP) knowledge
  • FDA Code of Federal Regulations knowledge
  • Valid US Driver's License with good record
  • Willingness to travel up to 60%
  • Bachelor's degree in Pharmacy or Life Sciences

Nice-to-have

  • Experience with Phase II and Phase III trials
  • Mentoring less experienced Site Managers
  • Process improvement contributions
  • Strong written and oral communication skills
  • Proactive problem solving abilities

Key Requirements

  • Minimum 2 years clinical trial monitoring experience
  • Minimum 2 years Oncology therapeutic area experience
  • Bachelor's degree in Pharmacy, Nursing, or Life Sciences
  • Valid Driver's License issued in one of the 50 United States
  • Knowledge of drug development process and FDA regulations

Work Rights

Not specified

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