Senior Site Manager, X-ta

Johnson & Johnson UK

High Wycombe, United Kingdom
Fully remote
Clinical trial protocol compliance
Gcp and regulatory adherence
Site monitoring and oversight
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

Job Summary

  • 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.
  • Activities range from site feasibility and selection over site initiation and start-up, to preparation and conduct of site monitoring, oversight of key performance indicators and site/study close-out in complex clinical trials.
  • We offer a competitive salary and extensive benefits package, a flexible working environment, and career development opportunities.

Matching Summary

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.

Skills & Requirements

Must-have

  • Clinical trial protocol compliance
  • GCP and regulatory adherence
  • Site monitoring and oversight
  • Data accuracy and completeness
  • Risk-based monitoring model

Nice-to-have

  • Strong communicator and problem solver
  • Quick learner and team player
  • Coaching and mentoring skills
  • Process improvement participation
  • Therapeutic area knowledge

Key Requirements

  • Minimum 3 years clinical trial monitoring experience
  • BA/BS degree in Life Sciences or related field
  • Strong understanding of GCP, local laws, and regulations
  • Proficient in English

Work Rights

Not specified

Tailored Resume

Cover Letter