Manager Data Management

GSK

Base: pln 255,750 to pln 426,250 gross annually; b...
Not specified
Clinical data management
Study database lock and archival
Sponsor oversight of outsourced studies
GSK is seeking a Manager of Data Management to oversee end-to-end study activities, ensuring quality and timely delivery of clinical data management tasks. The ideal candidate will have experience in clinical trials, with a strong understanding of data management strategies and regulatory compliance

Job Summary

  • GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together.
  • The role is accountable for the end-to-end data management and statistics & methodology study related activities including quality, delivery, and compliance with SOPs and regulatory guidelines.
  • The position offers a competitive salary range in Poland with additional benefits including private healthcare, paid leave, life insurance, and pension plans.

Matching Summary

Match Score: 85

GSK is seeking a Manager of Data Management to oversee end-to-end study activities, ensuring quality and timely delivery of clinical data management tasks. The ideal candidate will have experience in clinical trials, with a strong understanding of data management strategies and regulatory compliance.

Salary

Base: PLN 255,750 to PLN 426,250 gross annually; Bonus/Equity: Eligible for bonus and awards based on criteria; Benefits: Private healthcare, paid days off, life insurance, pension plan, parental leave

Skills & Requirements

Must-have

  • clinical data management
  • study database lock and archival
  • sponsor oversight of outsourced studies
  • data management strategy execution
  • compliance with ICH and GCP guidelines
  • project management discipline
  • global supplier partnership management

Nice-to-have

  • mentoring junior team members
  • subject matter expert in data standards
  • communication of technical topics to non-technical audience
  • building influential networks
  • operational excellence focus
  • knowledge sharing within data management community

Key Requirements

  • Bachelor’s Degree in scientific or business discipline
  • Pharma and/or CRO experience
  • Knowledge of ICH and GCP regulations
  • Experience with clinical trial data and laboratory data
  • CCDM certification is an advantage

Work Rights

Not specified

Tailored Resume

Cover Letter