Junior Real World Evidence Specialist

AstraZeneca

👻

Ghostometer: Reposted 1 time

This role has appeared 2 times on AstraZeneca's job board. It may be a ghost job — consider researching before investing time in your application.

Poland - Warsaw Onsite Development

Apply for this position

About this role

Brief Job Description

Member of the Country Medical Affairs Team supporting scientific evidence and data generation activities across therapeutic areas. This is an operational and supportive role, focused on executing tasks within RWE projects under the supervision of experienced specialists. Responsible for administrative support, operational coordination, ongoing monitoring of research project progress, as well as contributing to the development of research protocols and scientific publications under senior guidance.

Job Responsibilities:

Assist in conducting evidence gap analyses

Support the definition of study objectives, endpoints, inclusion/exclusion criteria, and data collection methods

Support day-to-day coordination of real-world data generation projects, including:

Vendor contracting processes

Maintaining detailed budget tracking spreadsheets for all assigned projects

Participation in feasibility processes (remote or on-site)

Preparation of ethics applications for submission

Site contracting processes

Start-up activities including site initiation visits preparation, site training materials, and internal user onboarding

Maintaining and organizing the Trial Master File (TMF)

Study documents preparation

Identifying operational risks and maintaining study risk registers

Design of Case Report Forms (CRFs) aligned with protocol requirements, ensuring data capture is consistent with study objectives

Set-up and maintenance of study systems

Study registration in public registries (e.g., ClinicalTrials.gov, EU PAS Register) and ensure timely updates

Tracking study progress including milestones, patient recruitment, and trial documentation

CRF data review, query processing, discrepancy management, and ad hoc report generation

Maintaining day-to-day operational communication with CROs, and other vendors

Organizing study project meetings, steering committee meetings, and investigator meetings

Assist in the preparation of scientific manuscripts, abstracts, and posters for peer-reviewed journals and congresses

Conduct systematic and targeted literature reviews

Typical Accountabilities (per AZ framework and regulatory expectations):

Support the Evidence Generation process for MC Poland under supervisor guidance

Participate in the preparation and delivery of AZ-generated evidence projects

Contribute to the timely delivery of research protocols and scientific publications in accordance with project timelines

Ensure all scientific outputs adhere to Good Publication Practice (GPP) guidelines, ICMJE recommendations, and AZ internal standards

Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to the role

Report potential issues of non-compliance

Support monitoring of milestones, reporting requirements, and budget spend

Requirements:

Essential

MD or Biology/Pharmacy/science-related Master’s degree

Experience in conducting RWE projects

Basic knowledge of market access, economic understanding, as well as knowledge of the motivations of involved stakeholders

Good project management skills

Understanding and ability to interpret clinical data

Good presentation and communication skills

Ability to work as part of a team with colleagues from other areas

Ideally experience in health economics and outcome research from the pharmaceutical industry

Ability to conceptualize and communicate content well

Analytical mindset, open, flexible and team-oriented personality

Very good English skills

Understanding of ICH-GCP principles and regulatory framework for observational studies

Effective time management skills

Good knowledge of MS Office (Word, Excel, PowerPoint)

Desirable:

MD, Master’s degree or PhD in epidemiology, health research methodology, biostatistics and/or data analytics.

Date Posted

16-lip-2026

Closing Date

23-lip-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.