Therapeutic Area Lead Oncology Gu-hem Vienna, Austria
vor 2 Wochen
**Location** Wien, Vienna, Austria
**Job ID** R-228988
**Date posted** 11/06/2025
**Therapeutic Area Lead Oncology GU-Hem**:
**Location - Vienna - Austria**
Are you ready to make a significant impact in the field of oncology? As a Therapeutical Area Lead, you will play a pivotal role in shaping scientific leadership and brand strategies within the oncology therapeutic area. This dynamic position involves both internal and external medical responsibilities, where your expertise will drive life cycle management and strategic initiatives. You will be accountable for delivering local medical affairs initiatives, fostering scientific partnerships, and ensuring alignment with commercial and market access strategies. Your leadership will guide a team of Medical Affairs Managers, Medical Advisors, and Medical Science Liaisons to execute the local medical brand plan effectively. Collaborate with various functions to ensure that medical activities meet the highest scientific and ethical standards, ultimately benefiting patients and healthcare professionals
**Accountabilities**:
In this role, you will be responsible for conducting activities that align with AstraZeneca's values and comply with the Code of Conduct. You will complete all required training on time and report any potential compliance issues. Your strategic partnership with cross-functional teams will be crucial in implementing the overall strategy for the therapeutic area. You will integrate scientific evidence to support brand strategies, identify opportunities for evidence generation, lead scientific communications, and ensure the integrity of medical evidence. Additionally, you will manage the TA budget, provide insights into patient needs, and maintain compliance standards. Your leadership will extend to managing a diverse team, fostering strategic partnerships, and driving operational excellence.
**Medical Management**:
- Acts as strategic and operative partner for implementation of the overall strategy for the TA in a cross functional model
- Integrates, interprets, and disseminates scientific evidence and content on AZ products and disease areas of focus to support the brand strategy and to support disease/product value messages to internal and external stakeholders.
- Identifies, prioritises, and reviews opportunities to generate evidence to clinically differentiate AZ products and better understand overall disease state management based on external stakeholder perspectives and the needs of AZ regions and markets
- Leads development of specific scientific communications activities e.g. conference symposia or specific scientific meetings sponsored by AZ, such as external physician or patient expert meetings
- Delivers the appropriate interpretation and preserves the integrity of medical evidence
- Is accountable for the development and execution of the medical affairs plan according to budget and timelines
- Is accountable for the overall TA budget and resource planning
- Works in a strategic partnership with the Marketing and Market Access departments, providing key input in the local operational brand strategy by ensuring input of KEE, customer insights and competitive intelligence
- Is responsible for the overall above-brand medical TA strategy
- Acts as the patient insight expert in the assigned disease and therapeutic area team by deeply understanding the unique needs, experiences, patient journey and relevant outcomes for patients
- Facilitates patient insight knowledge sharing by raising awareness about patient insight strategies and activities
- Maintains a good working knowledge of company standards on medicines promotion and supports the Nominated Signatories in ensuring compliance standards for external audiences
- Sustains a “patient focus” in all design and interpretation activities (i.e., internal stakeholders, regulators, payers, prescribers, patients)
- Keeps own knowledge of best practices and relevant developments up to date
- Responds to unsolicited Medical Information (MI) requests about approved or unapproved AstraZeneca products, or about unapproved uses of approved AstraZeneca products
- Works together with External Service Provider for MI to meet the requirements set in the local MI procedure
**People Management**:
- Provides strong leadership in managing the diverse office and field-based team.
- Coaches and develops the whole Team to develop best in class capabilities (scientific expertise, communication skills, business acumen)
- Responsible for supervising the TA Medical Affairs activities, ensuring operational excellence.
- Responsible for establishing robust strategic partnerships between the Medical Affairs team and other functions.
**Skills/Experience**:
- Good understanding of Pharmaceutical Development (e.g. Clinical Research and R&D strategy)
- Understanding of the latest technical, regulatory, policy and real-world evidence generation dimensions
- Proven experience and track record of strong content an
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