Central Monitoring Lead (18 Months)

GlaxoSmithKline

Poland
Base: pln 320,250 to pln 533,750 gross; bonus/equi...
Hybrid (2-3 days in the office)
Risk based quality management (rbqm)
Centralized monitoring (cm)
Data analytics (da)
GlaxoSmithKline is seeking a Central Monitoring Lead for an 18-month hybrid role in Poland, focusing on implementing Risk Based Quality Management (RBQM) and data analytics across clinical studies. The ideal candidate should have relevant experience and strong analytical skills, with an emphasis on collaboration and communication

Job Summary

  • Lead the implementation of Risk Based Quality Management (RBQM) across studies, focusing on Centralized Monitoring (CM) and Data analytics (DA) to ensure consistent application of RBQM principles.
  • Accountable for setting up and execution of CM with DA to enable timely quality study delivery and drive discussions with cross-functional teams for critical to quality measures.
  • Offers a hybrid working model with flexibility in working hours, a supportive environment, and a wide range of benefits including a bonus and other statutory and optional benefits.

Matching Summary

Match Score: 85

GlaxoSmithKline is seeking a Central Monitoring Lead for an 18-month hybrid role in Poland, focusing on implementing Risk Based Quality Management (RBQM) and data analytics across clinical studies. The ideal candidate should have relevant experience and strong analytical skills, with an emphasis on collaboration and communication.

Salary

Base: PLN 320,250 to PLN 533,750 gross; Bonus/Equity: Eligible for a 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

  • Risk Based Quality Management (RBQM)
  • Centralized Monitoring (CM)
  • Data Analytics (DA)
  • ICH GCP and regulatory requirements
  • Quality, safety, risk management

Nice-to-have

  • Collaborative environment
  • Passionate about delivering results
  • Eager to make a difference
  • Professional team

Key Requirements

  • 1-3 years' central monitoring experience
  • Experience with RBQM tools and data analytics
  • End-to-end clinical development experience
  • Fluent English speaking and writing
  • Understanding and compliance with ICH GCP

Work Rights

Not specified

Tailored Resume

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