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　　Job Description

　　OBJECTIVES:

　　Lead the in-field execution of the Therapeutic Area (TA) Medical Plan by engaging key external stakeholders and delivering medical education initiatives

　　Maintain a deep and up-to-date level of knowledge and understanding of the latest scientific/medical knowledge in the relevant therapeutic area by reviewing medical literature and attending conferences/courses or other relevant events

　　Share insights from key external stakeholders to internal cross-functional stakeholders as needed to facilitate development of the Brand and Medical Plans

　　Pursue field medical excellence and innovate for improved solutions with strategic impact

　　ACCOUNTABILITIES

　　STRATEGIC PLANNINGDevelop and execute TA-specific MSL scientific engagement plan aligned with the TA Medical Plan to guide field work

　　Ensure appropriate and effective external stakeholder management by utilizing objective, aligned scientific criteria to profile KOLs and creates and regularly updates the TA KOL list

　　Capture and share in-field medical insights or intelligence within compliance framework to support brand, medical and scientific strategy and business development

　　Identify educational opportunities that are aligned with Takeda’s medical education strategies

　　Drive new or improved initiatives with strategic impact to the organization

　　EXTERNAL STAKEHOLDER MANAGEMENTEstablish Takeda’s presence with KOLs and academic institutions in defined geographies for TAs of strategic interest to the company by identifying, developing, and fostering relationships with KOLs

　　Meet regularly with identified KOLs to provide ongoing, balanced scientific exchange related to on-label indications and disease states

　　Respond to HCP unsolicited requests for medical information (including off-label information) related for marketed Takeda products and Takeda pipeline products

　　Support scientific training of Takeda-contracted speakers by providing ongoing support and education as needed

　　MEDICAL EXPERTISEDevelop and implement key medical activities (e.g. Advisory boards, medical education and peer-to-peer training) independently

　　Create or support the development of medical/scientific materials and slide decks as needed (e.g. MSL slide decks and advisory board slides) and ensure the content is appropriately reviewed and approved as per Takeda policies

　　Provide medical booth and session coverage at scientific meetings and report information of strategic interest to cross-functional internal stakeholders

　　Deliver clinical presentations and medical information to external stakeholders upon request and as appropriate

　　Responsible for maintaining a deep and up-to-date level of disease and product knowledge through continuous education

　　Attend courses and industry meetings, read industry publications and discuss TA-related information with colleagues to keep up to date with developments within the pharmaceutical industry

　　CROSS-FUNCTIONAL COLLABORATIONContribute as a member of the Brand Team to achieve collective goals

　　Act as the field-based reference point of scientific and clinical expertise for cross-functional internal stakeholders (e.g. medical, regulatory, commercial, market access) through training and ad-hoc support

　　Serve as an ongoing, infrequent training resource for sales representatives as per requests by commercial or sales Training, utilizing approved training materials

　　CLINICAL RESEARCHSupport ongoing/future Company Sponsored Studies (i.e. provides LOC review of proposed CRO site lists, attends site visits, provides site/investigator feedback to clinical operations) following the appropriate requests from Area/Regional or Global clinical development

　　Manage unsolicited requests from HCPs for investigator-initiated research (IIR) proposals by providing appropriate investigator support as per Takeda SOP as well as engaging with Global colleagues on IISR proposals as appropriate

　　Support Medical Affairs Company sponsored research (MACSR) as needed including site identification • Support national disease registries and Real-World Evidence (RWE) projects for relevant disease areas as needed

　　COMPLIANCEEnsure all field scientific-medical communications are fair-balanced, based on appropriate scientific evidence, and compliant with local regulatory norms and internal compliance rules

　　Ensure compliance of all responsible activities to relevant laws and regulations as well as internal standards and SOPs

　　Complete all required training, activity documentation, expense reporting, and other administrative responsibilities

　　PATIENT-CENTRICITYProvide support and/or leadership in planning and implementation of patient access programs as needed and as per local regulatory requirements

　　Prioritize patient safety by following all PV-related processes

　　Support reporting of product-related medical safety issues by providing input on product-related quality issues and incidents to the local PV-team

　　QUALIFICATIONS:

　　Medical degree (M.D.), advanced degree in Life Sciences (e.g. Master, Ph.D., PharmD), or equivalent combination of education and experience

　　1 – 2 years of work experience in medical affairs, healthcare industry or academia

　　Prior MSL experience in relevant Therapeutic Area (oncology or hematology)

　　Clinical research experience is preferred

　　Excellent interpersonal skills with the ability to develop relationships easily, even with difficult people or situations

　　Excellent verbal and written communication skills in English and Mandarin (essential); fluency in other languages is a plus

　　Excellent oral presentation skills

　　Strong planning and organization skills with ability to prioritize • Independent and self-driven with a positive work ethic

　　Team player, collaborative and agile

　　Result-oriented with high sense of urgency and adherence to timelines

　　Meticulous and strong analytical skills

　　Ability to engender trust and respect of peers and superiors

　　Strong ethical and professional mindset

　　Well versed in highly technical and scientific languages

　　Proficient with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook

　　TRAVEL REQUIREMENTS:

　　Able to travel to various meetings/customer sites, including overseas travel (up to 70% of time)

　　At times will need to have overnight travel, including weekend commitments

　　Locations

　　Taipei, Taiwan

　　Worker Type

　　Employee

　　Worker Sub-Type

　　Regular

　　Time Type

　　Full time