Medical Affairs Scientist (Izmir Based) Full-time NEW

Medical Affairs Role

To provide deep medical & scientific expertise to support healthcare professionals, professional associations, patient groups and other relevant decision makers. This includes developing and delivering the local medical strategy and life-cycle clinical plans for Pfizer's inline and pipeline medicines in nominated therapy area, communicating the safe and appropriate use and the value of Pfizer medicines in order to improve patient outcomes, enhancing clinical practice and supporting business needs at the national, regional and corporate level, demonstrating the value of our innovative medicines, creating industry leading digital educational and scientific content that is timely, relevant, balanced, interactive, innovative and easily digestible, championing the patient voice when developing and implementing medical strategies, providing subject matter expertise and high-quality scientific exchange, bringing in insights into the organization to shape strategy, providing focused, relevant information in response to clinician needs and the needs of their patients, establishing Pfizer as a key research partner within National Life Sciences, establishing deep and lasting relationships with healthcare professionals and other relevant decision makers, creating constructive and effective cross-functional partnerships with internal departments and external stakeholders, providing medical & scientific expertise to healthcare professionals, professional associations, patient groups and other relevant decision makers through scientific communications, establishing Pfizer as a key research partner within National Life Sciences by building academic and research collaborations within the nominated therapy area, establishing deep and enduring peer-to-peer relationships with leading healthcare professionals and specialists, including on-traditional partners and key decision makers, understanding clinicians' insights around current standard of care and strengthening their knowledge of the value of our medicines to the patients and decision makers, liaising with healthcare professionals to effectively communicate and manage drug safety issues, providing specialist medical and scientific input to the nominated internal teams in order to support the appropriate use of Pfizer medicines and successful implementation of Pfizer's initiatives and programs, identifying data gaps for pipelines assets and developing local RWD/RWE for the demonstration of the value of our products and market access, acquiring and maintaining in-depth scientific expertise of Pfizer medicines within nominated therapy area as well as of key competitors (including those in development), delivering key medical and scientific activities within the medical plan, providing medical/scientific input into protocol feasibility assessments for clinical trial proposals, identifying appropriate investigators / sites for Pfizer-sponsored clinical trials, working together with clinical research colleagues and in collaboration with global teams to drive the timely completion of Pfizer-sponsored clinical trials, providing input into clinical development teams to ensure design and selection of trials relevant to Turkey needs, leveraging clinician, payer and patient insights, presenting high-quality, accurate, balanced and specific information to healthcare professionals and other relevant decision makers in response to unsolicited requests for information, creating industry leading and impactful scientific and medical content through a range of digital channels and formats that is timely, relevant, balanced, interactive, innovative and easily digestible, ensuring medical insights are brought into the organization to shape future strategies, leading local advisory boards to gain clinical and patient insights, working with patients and patient organizations to understand unmet medical need and to ensure the patient voice is at the center of medical strategies and projects, providing medical expertise into regulatory and market access strategies for pipeline assets, including early licensing & access schemes, regulatory and HTA submissions and adaptive pathways, providing medical expertise for regulatory labelling updates, risk management plans and license maintenance, providing clinical input to Medical Information to facilitate the maintenance of an accurate, relevant and high-quality database of standard response documents/creation of new responses, developing and maintaining strong cross-functional working between global and local country teams, identifying opportunities for customer focused digital solutions and contributing to their creation in partnership with MAS/Digital Medical, performing the medical customer facing activities for the assigned products, according to the priorities defined with the Manager, and liaising with the other medical colleagues, if applicable, reviewing and sign-off to ensure compliance of promotional materials and company sponsored activities such as local promotional meetings and events with local SPCs and requirements, working closely with the MAEL, MAS/Digital Medical, the MAS/Real World Data Expert, the Medical Quality Governance Manager (MQGM), Compliance, Legal and all cross-functional team, including customer-facing roles.