Member of Country Medical Affairs Team responsible for scientific evidence & data generation plans & activities across therapeutic areas and along product life cycle
Responsible for developing and implementing the Country Medical Affairs product-related scientific data generation plan & vision in support of the Country and Regional Medical Affairs and specific therapy area teams
Ensure data generation strategies alignment to overall TA strategies and LOC, including local Medical, Patient Value and Access and BU strategies, closely cooperate with cross functional teams
Oversee the processes,requirements, vendors( CRO, Clinical ResearchOrganisations)and budgets necessary for data generation, accountable for output and respective publications
Responsibilities:
Identifydata gaps (gap analysis) and createevidencegeneration plans in the context of drug development.
Alignmenof RWE strategy in collaboration with market access team and medical stakeholders of the relevant BU as well as EUCAN/global in the relevant therapeutic area (close coordination and collaboration with international and headquarters health economics and outcomes research teams, RWE & outcomes research teams)
Identification and coordination of projects/project management for the generation of real-world data (including, but not limited to):
Plan FMV/study budget
Contract vendors
Identifypotential sites
Conduct feasibility process (remote or onsite)
Compile ethics applications for submission
Support sites contracting
Track the progress of a studies including milestones, patient recruitment, trialsuppliesand trial documentation
Take operational and administrative responsibility for local studies and ESRs.
Track and process invoices and authorized payments to selected vendors and investigational sites, accurately andin a timely manner
Oversee study implementation and actively support the analysis and interpretation of real-world data in close collaboration with the external stakeholders involved
Identifyscientific partners and other relevant stakeholders and build resilient relationships with them
Support health economic analyses (modelingin the area ofhealth economics; cost effectiveness and budget impact analyses)
Effectively communicate concepts, project plans, studyresultsand lessons learned with external and internal stakeholders, as well as through scientific publications
Translates the strategic plan & vision of the LOC Medical Affairs andoverallTA Plan to create research and study designs for the generation of scientific evidence along the product lifecycle
Ensures processes, strategies, and planning tools related to data generation, as well as the output of statistics and writing
Puts in place data management plans, timelines and manages multiple projects through closeout and archiving
Designs Case Report Forms, support edit check specifications, support creation of test scripts and tests the related study databases, query processing, and data reporting
Leads study start-up activities like training sites, internalusersand study project meetings
Ensures study data quality by CRF data review, preparation for entry, query processing, discrepancy management, ad hoc reporting, listing generation
Creates andmaintainsall essential scientific data generation & management documentation
Performs as a point of contact with vendors such as CROs, Database developers, coders, Safety personnel,QAetc.
Typical Accountabilities
ExecuteEvidence Generation process for MC Poland
Executeend to end preparation,deliveryand dissemination of the AZ generated evidence
Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role. Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time. Report potential issues of non-compliance.
Ensuresappropriate trackingof milestones for AZ studies, compliance with reporting requirements and budget spend
Ensuresand monitor compliance by project team members and third parties by (a) positively reinforcing the Code of Conduct and all relevant AstraZeneca Policies and Standards, (b) ensuring completion of all required training, and (c)immediatelyaddressing and reporting, asappropriate, instances of non-compliance.
Accountability for GXP areas is expected.
Requirements:
Essential
MD or Biology/Pharmacy/science-relatedMaster’sdegree
Experience inconductingRWE projects
Basic knowledge of market access, economic understanding, as well as knowledge of the motivations of involved stakeholders
Good project management skills (experience in study management)
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
Ability to travel (up to 30%)
Ideally experience in health economics and outcome research from the pharmaceutical industry
Ability to conceptualize and communicate content well
Analytical mindset, open,flexibleand team-oriented personality
Very goodEnglish skills
Effective time management skills
Good knowledge of MS Office (Word, Excel, PowerPoint)
Desirable
MD,Master’sdegreeor PhD in epidemiology, health researchmethodology, biostatistics and/or data analytics
Date Posted
16-cze-2026
Closing Date
30-cze-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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