Senior Site Manager, Immunology

Johnson & Johnson

High Wycombe, Buckinghamshire, United Kingdom
Fully remote
Gcp and regulatory compliance
Site feasibility and selection
Clinical trial monitoring
Johnson & Johnson is seeking a Senior Site Manager for Immunology trials, a home-based position responsible for ensuring compliance with clinical trial protocols and overseeing site activities from initiation to closure. The ideal candidate will possess strong communication skills and a background in clinical trial monitoring, preferably with experience in the immunology therapeutic area

Job Summary

  • As a Senior Site Manager, you will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure.
  • You will be responsible for oversight of clinical trial protocols at a site level and will collaborate closely with a Local Trial Manager (country project manager), Clinical Trial Assistant, and Clinical Trial Manager (regional project manager).
  • We offer a competitive salary and extensive benefits package, a flexible working environment, and career development opportunities.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Site Manager for Immunology trials, a home-based position responsible for ensuring compliance with clinical trial protocols and overseeing site activities from initiation to closure. The ideal candidate will possess strong communication skills and a background in clinical trial monitoring, preferably with experience in the immunology therapeutic area.

Skills & Requirements

Must-have

  • GCP and regulatory compliance
  • Site feasibility and selection
  • Clinical trial monitoring
  • Data accuracy and completeness
  • Recruitment and retention strategies

Nice-to-have

  • Strong communication and influencing skills
  • Teamwork and problem-solving
  • Independent work ethic
  • Therapeutic area knowledge

Key Requirements

  • 3 years of clinical trial monitoring experience
  • BA/BS degree in Life Sciences or related field
  • Ability to establish a home office
  • Willingness to travel up to 50%

Work Rights

Not specified

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