By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda'sPrivacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job DescriptionJOB FUNCTION Provide medical expertise and support for Therapeutic Area(s) (TAs)/Takeda products with responsibility to Market Access, Brand Management / Marketing & KAMs and other internal stakeholdersSupport the TA Medical Head/Lead and Medical Science Liaisons (MSLs) in establishing the local Medical Strategy Plan and its implementation for the TA of responsibilityEnsure the correct interpretation and communication of scientific data of Takeda productsPlay a role of advocate for patients needsAssist with launch of new products in marketACCOUNTABILITIES Medical/Scientific AffairsContinuously screen, review and analyse scientific literature; generate summaries & critical assessments if appropriatePresent the clinical evidence to internal and external stakeholders in a non-promotional way, e.g. reimbursement bodies, while determining their and patient needs in order to become a partner in improving health careAssess scientific accuracy and validity of promotional and non-promotion material and its compliance with Takeda standards, SOPs and national lawsIn collaboration with TA Medical Head /Lead, define, supervises approval process and implement specific medical programs and activities (e.g. medical meetings, disease state education, advisory boards) and associated resource requirements and budgetsManage and approve commercial activities according to TA interests and Takeda legal and compliance requirements and policies.Communicate and align with Regional and Global Medical Affairs functions, as well as with other LOC functions (e.g. Commercial, Market Access) to ensure alignment in meeting customer needsDevelop local strategic medical plans in line with product Life Cycle Management plans and oversee execution (including the production of local publications, planning and conduct of local Advisory Board meetings etc.)Establish and maintain strong relationships with Key Opinion Leaders (KOLs), understand their needs in order to segment them and create medical strategy and tactics per segment accordinglyAct as communication link to authors of scientific publications about Takeda productsProvide extensive, clear and structured briefing to external presenters/speakers at Takeda sponsored medical events, e.g. local Advisory Boards, doctors' meetingsIdentify gaps in the local clinical study program which are a hurdle for successful regulatory and/or clinical acceptance of the product and propose studies to address these issueProvide medical expertise to LOC Market Access, e.g. Pricing & Reimbursement Dossier creationProvide medical expertise to LOC Regulatory Affairs/LOC Pharmacovigilance/LOC Quality AssuranceEvaluate and support local investigator initiated research proposals in alignment with global strategy and Takeda standards and SOPsBudget responsibility for medical affairs activities related to TA/productOther medical and scientific support duties as assignedProvide medical training for allocated therapeutic area / products to Marketing & SalesProvide scientific input into Marketing strategy and tacticsProvide medical input for development of promotion materialAssess scientific accuracy and validity of promotion material and its compliance with Takeda standards, SOPs and national laws and regulationsCROSS-FUNCTIONAL COLLABORATION Ensure awareness and communication of medical activities to other departments within the Local organizationParticipate in local product committees and brand planning cycles; owner of medical part of brand planCLINICAL DEVELOPMENT Develop study outline and protocol for local post-authorization (phase 4) and other RWE studies sponsored by Takeda; coordinate/oversee study conduct, data analysis and disclosure, reporting/publicationLiaise with CROs and other vendors for Takeda sponsored global studies as appropriate being able to do supervision to fulfil with regulations regarding local studies.Collaborate with Global Development Operations functions (e.g. LOC Support)MEDICAL INFORMATION Provide timely, accurate and balanced answers to unsolicited medical enquiriesCollaborate with Regional and Global Medical InformationOTHERS Promote, encourage and demonstrate commitment to Takeda-ism philosophy and valuesCommunicate any adverse reaction as soon as it is identified to the Pharmacovigilance Department as detailed in the company's internal proceduresAct according to Corporate, Compliance, Ethical codes and Legal standards.LocationsMadrid, SpainWorker TypeEmployeeWorker Sub-TypeFixed Term (Fixed Term)Time TypeFull time
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