Medical Therapy Area Lead – GI/HAE, East Gulf & Levant
応募 後で応募 求人ID R0162913 掲載日 09/15/2025 Location: United Arab EmiratesBy 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 Noticeand 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
About the Role
The Medical Therapy Area Lead is the most senior role on the Medical Affairs team and reports directly into the country Medical Head. The TA Lead is responsible for developing and executing Medical Affairs strategies for the East Gulf and Levant cluster in the Gastroenterology and Hereditary Angioedema (HAE) therapeutic areas. This role plays a pivotal part in shaping and implementing strategic medical plans that support Takeda’s mission of delivering better health and a brighter future. Success will depend on strong cross-functional collaboration with Commercial teams, alignment with Area and Regional Medical functions, and building trusted partnerships with external stakeholders.
How you will contribute:
Scientific Leadership
Craft and execute the medical communication plan. This includes delivering medical education and developing scientific platforms,
Earn and maintain credibility through continuous learning, thought leadership, and presence in professional forums
Provide strong medical insights to inform clinical research activities and contribute to evidence generation strategies.
Stakeholder engagement
Identification & Segmentation: Define specific objectives and determine which stakeholder groups can help achieve them.
Segment stakeholders, including KOLs, HCPs, payers, regulators, patient groups, and digital opinion leaders, by their roles and influence level.
Conduct mapping exercises to understand each stakeholder’s interests and potential impact.
Develop and implement TL engagement programs, particularly in pre-launch and launch phases.
Build strong partnerships with healthcare professionals, scientific societies, and patient groups (where applicable).
Drive advisory boards, scientific partnerships, and publication strategies to shape treatment pathways and patient care.
Support product registration, and formulary inclusion.
Ensure robust pre-approval and launch readiness activities in collaboration with Commercial and cross-functional teams.
Organizational Excellence:
Approve promotional and non-promotional materials, activity, and engagement requests
Establish and maintain a culture of compliance, ensuring adherence to Takeda’s Code of Conduct, local regulations, and industry best practices.
Oversee implementation and compliance with Medical Affairs SOPs
Ensure timely follow-up, tracking, and reporting of adverse events in accordance with PV standards.
Serve as a strategic bridge for aligning priorities across functions
Lead Medical Affairs input into Named Patient Programs and early access initiatives.
Design and execute regular audits of Medical Affairs processes to ensure compliance and operational excellence.
Implement corrective actions and continuous improvement initiatives as required
Use virtual tools: online forums, digital opinion leaders (DOLs), webinars, AI-powered chatbots, and e-learning modules.
Adhere to allocated budget and ensure funds are directed toward high-value activities that advance scientific and patient objectives.
Major Challenges
Supporting multiple new product launches and indications in a fast-paced environment.
Building medical capabilities in new therapeutic areas
Ensuring effective cross-functional collaboration and alignment across local, regional, and global teams.
Establishing Medical Affairs as strategic business partners across the organization.
Qualifications & Experience
Medical advisor level and above
Medical degree (PharmD, PhD, or MD or equivalent) required; relevant postgraduate degree (e.g., Master’s degree in a specialty) strongly preferred.
Experience in gastroenterology or rare diseases strongly preferred
Experience managing multiple countries with diverse healthcare systems, strongly preferred
Minimum 10 years’ professional experience, including at least 5–6 years in Medical/Scientific Affairs within a reputable mid- to large-sized organization.
Demonstrated experience leading teams, driving medical strategy, and managing stakeholders across complex healthcare environments.
Required Capabilities
Strategic thinker with strong innovation and execution capabilities.
Proven ability to manage multiple complex initiatives under pressure.
Exceptional leadership, coaching, and team development skills.
Strong interpersonal, communication, and relationship-building abilities.
Goal-oriented, energetic, and resilient.
Highly process- and compliance-oriented.
As an expert professional within the organization, you develop innovative solutions to complex problems aligned with organizational objectives. Your work involves addressing intricate issues, requiring in-depth analysis and judgment. You also engage with key contacts outside your expertise area and contribute to the development of new concepts and standards. Operating with considerable autonomy, you serve as a consultant to management and an external spokesperson on major matters, often working independently and leading function teams or projects. Additionally, you play a role in training and mentoring junior staff.