Study Manager

GlaxoSmithKline

Poland
Base: pln 186,750 to pln 311,250 gross; bonus/equi...
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Clinical study delivery process
Ich-gcp and regulatory requirements
Vendor and cro oversight
** GSK is seeking a Study Manager in Poland to lead and coordinate clinical studies from planning to close-out, ensuring compliance with standards and effective communication among teams. The role offers opportunities for professional growth and emphasizes a collaborative work environment. **

Job Summary

  • Lead and coordinate the delivery of clinical and evidence generation studies from planning through close-out.
  • Monitor study conduct and progress, identify, resolve and escalate risks/issues.
  • This role offers growth through exposure to global study delivery, the chance to shape ways of working, and meaningful impact aligned with our mission of uniting science, technology and talent to get ahead of disease together.

Matching Summary

Match Score: 75

** GSK is seeking a Study Manager in Poland to lead and coordinate clinical studies from planning to close-out, ensuring compliance with standards and effective communication among teams. The role offers opportunities for professional growth and emphasizes a collaborative work environment. **

Salary

Base: PLN 186,750 to PLN 311,250 gross; Bonus/Equity: Eligible for bonus and/or awards for exceptional performance; Benefits: Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus, private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave

Skills & Requirements

Must-have

  • Clinical study delivery process
  • ICH-GCP and regulatory requirements
  • Vendor and CRO oversight
  • Budget tracking and management
  • eTMF inspection readiness

Nice-to-have

  • Agile model collaboration
  • Global study delivery exposure
  • Shaping ways of working

Key Requirements

  • 3+ years of relevant work experience
  • Knowledge of clinical trials and drug development
  • Strong knowledge of ICH-GCP
  • Project management skills
  • Excellent verbal and written communication in English
  • Microsoft Office and CTM systems proficiency

Work Rights

Not specified

Tailored Resume

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