Global Study Director, Late-Development Oncology Programs

AstraZeneca GmbH

Warszawa

On-site

PLN 200,000 - 320,000

Full time

8 days ago

Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Job summary

AstraZeneca is seeking a Global Study Associate Director (GSAD) in Warsaw, Poland, to lead cross-functional study teams and drive study delivery in late development oncology. You will ensure timelines, budget, and quality while partnering with CPT and external partners.

Essential requirements include 7+ years in clinical research with project management experience, strong leadership, and regulatory knowledge. This is a strategic, field-facing role requiring collaboration across global teams.

Qualifications

University degree (or equivalent) in medical/biological sciences or related discipline.
7+ years of relevant clinical experience in pharma, including 2+ years in project management.
Strong knowledge of clinical research regulatory requirements and study management processes.
Solid project management skills and familiarity with relevant tools.
Strong leadership and ability to build effective working relationships.

Responsibilities

Lead cross-functional study teams to deliver clinical milestones on time and within budget.
Facilitate communication across functions and provide guidance to core and extended study team members.
Serve as AZ point of contact for CROs for outsourced studies, ensuring oversight and timely delivery.
Contribute to development of essential study documents (CSP to CSR) per AZ SOPs.
Oversee TMF completion and ensure regulatory governance and quality controls.
Monitor study plans, KPIs, and risk management; escalate issues with mitigation plans.