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’s Privacy 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 Description** **Job Purpose** Act as a trusted scientific partner in the field by engaging healthcare professionals in peer-to-peer scientific exchange, driving insights collection, and supporting local evidence generation, under the strategic guidance of the Medical Manager and in alignment with the Medical Affairs plan. **Role Core Responsibilities & Accountabilities** + Establish and maintain peer-to-peer relationships with HCPs, acting as a scientific resource and trusted partner in assigned territory. + Plan and execute territory-level KOL engagement aligned with the local medical plan, brand strategy, and scientific priorities. + Facilitate timely, accurate, fair-balanced scientific exchange and medical education aligned with compliance standards. + Gather, analyze, and share actionable medical insights from HCPs to inform cross-functional planning and R&D alignment. + Represent Takeda at scientific meetings and congresses, providing internal summaries and follow-up insights. + Deliver training on disease area, clinical data, and product information to commercial, access, regulatory, and patient services colleagues. + Provide scientific support for company-sponsored clinical trials and investigator-initiated research, including feasibility, site interaction, and education. + Maintain updated knowledge of therapeutic area and treatment landscape, contributing to internal medical intelligence. + Accurately document field activities and HCP interactions using CRM tools, ensuring alignment with SOPs and compliance policies. + Collaborate with cross-functional teams to support local initiatives such as advisory boards, speaker training, and patient-focused projects. **Role Mandatory Responsibilities** + To act in-line with Takeda’s “Information Security Policy” and “Acceptable Use of Technology Policy”. + Being a Quality and Safety Ambassador by identifying and promptly communicating product quality and pharmacovigilance issues to appropriate internal teams. + Excels in ethical behavior by consistently acting with integrity and serving as a role model for Takeda-ism values and ethical decision-making. + Training & Compliance: Ensure full and timely completion of all mandatory Takeda training requirements and compliance with global, regional, and local procedures and SOPs. + Speak-up for Integrity: Encourage a culture of openness by raising any concerns in good faith via the Ethics Line, to line management or directly to Ethics & Compliance. Job Dimension + OPEX responsibility: YES + Financial Responsibility: YES + Volume Impact: No + Revenue Impact: No Role required Qualifications & Capabilities + University degree in Medicine or Pharmacy, advanced scientific degree preferred. + Demonstrated ability to effectively engage and communicate with KOLs and external medical stakeholders. + Highly qualified presentation skills + Strong verbal and written communication skills in English and local language. + Understanding of relevant therapeutic area, clinical data interpretation, and real-world evidence. + Excellent planning, time management, and prioritization skills in a remote/field-based setup. + Digital literacy in CRM systems, Microsoft Office, and virtual communication tools. + Strong ethical standards and compliance-driven mindset. + Minimum 2 years of experience in Medical Affairs or relevant clinical/research environment in the pharmaceutical industry is preferred. **Locations** Istanbul, TurkeyAnkara, Turkey **Worker Type** Employee **Worker Sub-Type** Regular **Time Type** Full time