Hybrid Associate Director, Global Study Lead

Posted 4 minutes ago

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About the role

  • Lead global clinical studies in a biopharma company aimed at improving public health. Collaborate with cross-functional teams to ensure quality and compliance in study delivery.

Responsibilities

  • Lead the planning and delivery of a global clinical study.
  • Act as the point of accountability for study delivery, quality and risk management from setup to archive.
  • Define and drive the study delivery plan, including feasibility, timelines, data capture strategy and quality controls.
  • Lead and coordinate cross-functional and vendor teams to ensure on-time and compliant study execution.
  • Identify, assess and manage study risks; escalate issues and implement mitigation plans.
  • Contribute to protocol development and regulatory submissions.

Requirements

  • Bachelor’s degree in life sciences, pharmacy, nursing, medicine or a related discipline.
  • Minimum 5 years’ experience in clinical development, clinical operations or study management in industry or CRO.
  • Proven experience leading global study setup and delivery across multiple countries.
  • Solid knowledge of Good Clinical Practice and clinical trial regulations.
  • Experience managing outsourced vendors and external partners for study execution.
  • Fluent English, with strong written and verbal communication skills.

Benefits

  • Private healthcare
  • Additional paid days off
  • Life insurance
  • Private pension plan
  • Fully paid parental leave & care of family member leave

Job title

Associate Director, Global Study Lead

Job type

Experience level

Senior

Salary

PLN 339,750 - PLN 566,250 per year

Degree requirement

Bachelor's Degree

Location requirements

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