Associate Medical Evidence Advisor Lung Cancer (Maternity Leave) at AstraZeneca

Milan, Lombardy, Italy -

Full Time

Start Date

Immediate

Expiry Date

20 Feb, 26

Salary

0.0

Posted On

22 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Degree, Scientific Degree, Clinical Research, Project Management, Communication Skills, Team Working, Networking, Statistical Analysis, Health Outcomes, Evidence Generation, Drug Development, Market Access, Data Protection, Budget Management, Clinical Trials, Healthcare Systems Knowledge

Industry

Pharmaceutical Manufacturing

Description

Are you ready to make a difference in the world of oncology? As a Associate Medical Evidence Advisor Lung Cancer within the Italian MC, you'll be at the forefront of identifying Real World Evidence (RWE) needs and bridging gaps in the evidence base. Reporting to the Oncology Medical Evidence and Medical Excellence Head, you'll collaborate closely with local cross-functional brand teams to align evidence strategies with brand objectives. Your strategic insights will empower timely responses to external customer requests, while your extensive knowledge of databases will ensure relevant information is at your fingertips. You'll also build strategic relationships with partners and third-party vendors, ensuring robust information governance and data protection. Join us in contributing to Externally Sponsored Research (ESR) and driving impactful evidence activities in alignment with AstraZeneca's strategy. This role is based in Milan. Accountabilities What you'll do: Be the RWE point person for identifying research needs within the Holistic Evidence Strategy for prioritized brands. Develop specific RWE research programs to support market access and scientific knowledge. Ensure quality and performance standards for research projects are realistic and attained. Bridge medical, market access, and commercial agendas by establishing evidence requirements. Demonstrate understanding of drug development and post-marketing support for RWE strategy. Manage projects/programs, including budget and resources, with Medical and Payer perspectives. Assess feasibility of study proposals for both ESR and AZ Sponsored observational research. Coordinate internal project review and governance processes for initiatives and ESR proposals. Communicate and collaborate with Global & Regional counterparts, experts, and stakeholders. Ensure data access and collection in RWE studies. Maintain quality assurance in Evidence Generation Studies. Apply technical expertise in statistical analysis, economic models, clinical trials, and more. Write relevant sections of Study Design Concepts, Protocols, Reports, and Manuscripts. Effectively communicate health outcomes information to partners, the scientific community, and customers. Lead dissemination of health outcomes information through abstracts, posters, and manuscripts. Ensure ethical applications and interaction with authorities regarding healthcare data/registries. Register studies in applicable systems and post results according to Transparency policy. Write and negotiate agreements with scientific consultants, investigators, service providers, etc. Initiate collaboration with external investigators, clinicians, payers, consulting companies, etc. Facilitate study drug supply and ensure patient safety reporting in ESR projects. Collaborate with AstraZeneca's other MCs, Regional & Global Medical Affairs, R&D regarding Evidence activities. Contribute to responses for access issues related to pricing, reimbursement, and access initiatives. Assure correct quality in accordance with procedures, legal requirements, and internal standards. Manage activities and account relationships according to Company Values, Code of Conduct, Guidelines/Internal procedures, and Italian legislation. Essential Skills: Medical Degree or Scientific Degree in relevant TAs Fundamental knowledge of basic research, drug discovery, drug development, clinical environment Previous experience in clinical research Knowledge of Clinical Research legislation Knowledge and experience of local healthcare systems and language Proficiency in spoken English Good knowledge of Microsoft Office (especially Excel and PowerPoint) Demonstrated Project Management skills Project Management Leadership Communication and public speaking skills Goal oriented Team working and cross-functional capabilities Networking with internal and external stakeholders Desirable Skills Master’s degree or equivalent in science/healthcare related field Qualified Doctor An active interest in pursuing continuing education within the Pharmaceutical Industry Experience in a pharmaceutical industry Digital & AI skills: experience applying AI/ML (including NLP and generative AI) to RWE analyses When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are committed to transforming the practice of medicine by generating compelling medical evidence that improves patient experiences. Our collaborative culture fosters openness and transparency while empowering individuals to drive their career development. By leveraging diverse skills across teams, roles, and levels, we advance our pipeline and redefine cancer treatment. Join us in making a significant impact on patients' lives through innovative scientific evidence. Ready to take on this exciting challenge? Apply now to become part of our dynamic team! Date Posted 21-nov-2025 Closing Date 05-dic-2025 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.

Responsibilities

The Associate Medical Evidence Advisor will identify Real World Evidence needs and develop research programs to support market access and scientific knowledge. They will manage projects, ensure quality standards, and collaborate with various stakeholders to drive impactful evidence activities.