Specialist I/Specialist II, Evidence Project Management, Oncology in Warsaw

The Medical Evidence Delivery Team within Oncology Business Unit (OBU)

is responsible for strategic planning and operational delivery of interventional and observational AstraZeneca sponsored studies (AZ studies), externally sponsored scientific research (ESR) and early access programs (EAP) in order to generate the evidence to build confidence in and provide access to AstraZeneca therapies for patients in need.

Specialist, Evidence Project Management (Spec EPM)

will support the Associate Director, Evidence Project Management (AD EPM) and Manager, Evidence Project Management (Mgr EPM) in the operational delivery and oversight of company sponsored evidence studies and/or early access programs (EAP) to time, cost and quality. The Spec EPM works cross-functionally with internal and external partners to deliver certain aspects of the clinical study as delegated by the AD EPM/Mgr EPM and in accordance with the clinical outsourcing model (EMPOWER), current clinical trial regulations (e.g. ICH GCP), AstraZeneca Standard Operating Procedures (AZ SOPs), AZ policies and best practices and in line with AZ values and behaviours.

Responsibilities:

Maintain Study Inspection Readiness Tool

Coordinate and oversee periodic study-level TMF/Master File (MF) QC

Perform Periodic TMF/MF QC on behalf of Study/EAP Management

Customization of the study’s Expected Document List (EDL) in collaboration with the CROs

Collaborate with extended study team to develop, maintain, and execute activities according to the study Sponsor Oversight Plan

Ensure appropriate documentation of oversight and inspection-readiness tasks is maintained

Ensure handover documents are created, signed and filed in TMF

In collaboration with CRO, support creation, execution and maintenance of AZ TMF/MF Plan

Supports key study start-up activities, in collaboration with CRO and internal functions as needed

Internal system’s set up (VCV, SPOL, Shared mailbox, etc.)

D-code requests

Creation and maintenance of Study Team Charter / R&R document

Creation and maintenance of study team contact list

Creation and maintenance of Decision and Issue trackers Coordination & documentation of internal study team meetings

Provide input into development of study/EAP plans and study/program documents as needed

Support compliance and quality deliverables

Assist recording of QIs in VQV

Assist in audit/inspection preparation as needed

Monthly review of the data present in PharmaCM

Monthly review of workbooks

Create and maintain internal study/program trackers and systems as needed, including mailboxes and collaboration forums

Ensure new team members have access to all required systems

Enter/maintain accurate data relating to study/EAP scope and progress on all business systems throughout the course of study every month

Support budget management activities including

Raise POs

Maintain

Support invoice reconciliation

EAP program participation, status and tracking

creation of country tracker aligned with agreed country participation timelines/exit strategy

creation and maintenance of study team contact list

creation and maintenance of Decision and Issue trackers

Provide program level tracking and updates

Validate source information for stakeholder reporting

Maintain SSI with approved protocol

US specific local operational requirements

Ensure EAP MF Archiving

Active participation in CRO operational governance meetings

Requirements: Essential:

Bachelor’s degree required preferably in medical or biological science or equivalent by experience

Knowledge and understanding of the clinical study and drug development processes, GCP/ICH guidelines

Excellent written and verbal communication skills as well as proven collaboration and influencing skills

Team oriented and flexible; ability to respond quickly to shifting demands and opportunities

Demonstrated ability to collaborate as well as work independently

Ability to effectively work with Clinical Research Organisations/External Providers

Proven ability to interact widely and effectively within the company across regions, functions and cultures

Ability to manage competing priorities

Desirable:

Advanced degree in medical or biological sciences or field associated with clinical research

Proven organizational and analytical skills

Previous administrative training/experience

Date Posted 05-lis-2026

Closing Date 11-lis-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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