Associate Site Manager

Johnson & Johnson

Warsaw, Masovian, Poland
Fully remote
0-2 years clinical trial monitoring experience
Good clinical practice (gcp) compliance
Site initiation and close-out activities
This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness

Job Summary

  • This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness.
  • The Associate, Site Manager is responsible for executing site management activities from start-up through to site closure according to SOPs.
  • Candidates must ensure all Adverse Events are reported within required timelines and that data collected at trial sites is accurate and complete.

Matching Summary

This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness.

Skills & Requirements

Must-have

  • 0-2 years clinical trial monitoring experience
  • Good Clinical Practice (GCP) compliance
  • Site initiation and close-out activities
  • Adverse Event reporting timelines
  • Data accuracy and validity verification

Nice-to-have

  • Therapeutic area specific experience
  • Process improvement contributions
  • Leadership in team meetings
  • Analytical risk-based monitoring model
  • Strong IT skills in company systems

Key Requirements

  • BA or BS degree in Pharmacy, Nursing, or Life Sciences
  • Minimum 1 year of clinical trial monitoring experience
  • Proficiency in English and local country language
  • Willingness to travel with occasional overnight stays

Work Rights

Not specified

Tailored Resume

Cover Letter