Reporting to the Head of Medical Evidence and Medical Information, the Medical Evidence Advisor will be responsible for conducting local RWE AZ-sponsored studies and managing all operational activities related to supporting Externally Sponsored Research projects (ESR) in the Respiratory Biologics &amp; Immunology therapeutic area. Are you ready to make a significant impact in the field of medical evidence?Accountabilities- Accountable for the entire Evidence Generation Planning process, ensuring its strategic alignment with the Brand Strategy Plan process - Leader of the local evidence cross-functional study team (Med Affairs, Market Access, Marketing) to ensure delivery of Payer and Medical Evidence Generation studies - Accountable for coordination and management of RWE AZ-Sponsored studies (including primary and secondary data studies) with External Providers (CRO or database/registry holder) - Primary point of contact between the Company and the Investigator for ESR (externally sponsored research), coordinating all internal project review &amp; governance processes for ESR approval and guaranteeing delivery according to approved budget and timelines - Develop and maintain contacts with relevant Medical and Payer external stakeholders: KEEs, Scientific Societies, Pharmaco-epidemiologists, etc. - Accountable for local implementation of Global-led or Region-led RWE umbrella programs - Writing relevant sections of Study Design Concepts, Study Protocols, Case Report Forms, Study Reports, and Manuscripts for Publications - Communication and collaboration with Global &amp; Regional counterparts, experts, and stakeholders - Write and negotiate Agreements with service providers and others as applicable - Facilitate study drug supply and ensure patient safety reporting, as applicable, in ESR projects - Training of interns and new-in-role colleagues on Medical Evidence delivery processes and SOPs (ESRs, AZ-sponsored studies, Primary &amp; Secondary data studies; database studies, AZ publication procedures) - Acting as the Local Publication Coordinator within the Respiratory Biologics &amp; Immunology therapeutic area - Execution of all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations, and industry codes - Management of all activities and Account relationships according to Company Values, Code of Conduct, Guidelines/Internal procedures, and Italian legislationEssential Skills/Experience- Medical Degree or Scientific Degree and PhD in a relevant TAs - Fundamental knowledge of basic research, drug discovery, drug development, clinical environment - Previous experience in clinical research and as Clinical Project Leader or Clinical Trial Coordinator or Study Physician in pharmaceutical industry, health care or research environment - Relevant experience (at least 1/2 years) in a pharmaceutical industry - Excellent knowledge of Clinical Research legislation in particular for observational study and no-profit study - Proficiency in spoken English and Italian - Good knowledge of Microsoft Office (especially Excel and PowerPoint) - Project Management Leadership - Communication and public speaking skills - Goal-oriented - Team working and cross-functional capabilities - Networking with internal and external stakeholdersDesirable Skills/Experience- Experience in epidemiology and data analytics - An active interest in pursuing continuing education within the Pharmaceutical Industry - Experience in digital health and digital technologies in clinical research - Previous experience in Real-world evidence studiesWhen 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.AstraZeneca offers an environment where you can be at the forefront of medical innovation. We use our unique position as medical leaders across our enterprise and the healthcare ecosystem to shape the future of healthcare. Here, you will find endless opportunities to grow professionally while making a real difference in patients' lives. Our collaborative culture ensures that you will work alongside passionate colleagues who are dedicated to transforming healthcare through scientific excellence.Ready to make a difference? Apply now to join our dynamic team!Date Posted21-feb-2025Closing Date07-mar-2025AstraZeneca embraces diversity and equality of opportunity. &nbsp;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. &nbsp;We believe that the more inclusive we are, the better our work will be. &nbsp;We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. &nbsp;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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AstraZeneca

AstraZeneca, a leader in medical innovation, seeks a full-time Medical Evidence Advisor with a Medical or Scientific Degree and PhD. The candidate will manage RWE AZ-sponsored studies and ESR projects in Respiratory Biologics & Immunology. We offer a collaborative culture with professional growth opportunities and flexible working arrangements, including in-office and remote work options.

Medical Evidence Advisor

Summary