Study Manager

Pharmajobber

Poland
Pln 186,750 to pln 311,250 gross; bonus/equity: el...
Hybrid
Clinical trial delivery process
Ich-gcp compliance
Vendor management
Lead and coordinate the delivery of clinical and evidence generation studies from planning through close-out, ensuring studies are on time, on budget, and compliant with standards

Job Summary

  • Lead and coordinate the delivery of clinical and evidence generation studies from planning through close-out, ensuring studies are on time, on budget, and compliant with standards.
  • Monitor study conduct, resolve risks/issues, draft key clinical documents, and coordinate with internal teams and external partners.
  • Oversee budget tracking, eTMF readiness, and clinical supply delivery, while actively contributing to Study Leadership and Central Study Teams.

Matching Summary

Lead and coordinate the delivery of clinical and evidence generation studies from planning through close-out, ensuring studies are on time, on budget, and compliant with standards.

Salary

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, fully paid parental leave & care of family member leave

Skills & Requirements

Must-have

  • Clinical trial delivery process
  • ICH-GCP compliance
  • Vendor management
  • Budget tracking
  • eTMF inspection readiness

Nice-to-have

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

Key Requirements

  • 3+ years of relevant work experience
  • Knowledge of clinical trials
  • Strong ICH-GCP knowledge
  • Project management skills
  • Excellent English communication

Work Rights

Not specified

Tailored Resume

Cover Letter