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Central Monitor

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GSK

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Location:
Poland , Warsaw

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

269250.00 - 448750.00 PLN / Year
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Job Description:

You will join the Central Monitoring team in Poland to support Risk Based Quality Management across global clinical studies. You will review study data centrally, use data analytics to find trends and risks, and work with study teams to reduce those risks. We value curious problem-solvers who communicate clearly, learn quickly, and act with care for patients and data quality. This role offers strong learning and career growth and the chance to make a measurable impact by improving how clinical research protects participants and delivers reliable results. You will help unite science, technology and talent to get ahead of disease together.

Job Responsibility:

  • Perform centralized monitoring of study data from study start through database lock, following the study monitoring plan
  • Use data analytics tools to identify trends, data quality issues, and risks at site, country, and study levels
  • Communicate findings and recommended actions to study teams and support timely issue resolution and escalation
  • Maintain documentation and achieving central monitoring reviews and ensure inspection readiness
  • Support setup and ongoing maintenance of data analytics tools used for centralized monitoring
  • Train and coach central and local study teams on central monitoring processes and Risk Based Quality Management principles

Requirements:

  • Bachelor’s degree in life science, health, statistics, or related discipline
  • Minimum 3 years’ experience in clinical trials, clinical operations, or a related role within pharma, CRO, or academic research
  • Experience with clinical data review or centralized monitoring activities
  • Working knowledge of ICH Good Clinical Practice (GCP) and clinical research regulations
  • Strong written and verbal communication skills in English
  • Ability to work collaboratively across global and local teams and manage multiple priorities

Nice to have:

  • Familiarity with Risk Based Monitoring and Risk Based Quality Management concepts
  • Experience with centralized monitoring or data analytics tools (for example Spotfire, Clue Points, or similar)
  • Basic programming or data skills such as SQL, R, or Python, or experience interpreting statistical outputs
  • Experience working across multiple countries or time zones
  • Strong stakeholder management, influencing, and coaching skills
What we offer:
  • Performance with Choice – flexibility in working mode (hybrid working model 2/3 days per week in the office), flexible working hours
  • Established job in an international, well-known pharmaceutical company
  • Opportunity to work in professional team playing crucial role in maintaining GSK portfolio on the markets
  • Opportunity to work within GSK standards and documentation applied globally
  • Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus)
  • Supportive & friendly working environment

Additional Information:

Job Posted:
January 31, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
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