Therapeutic Area Lead CVRM Hungary will be responsible for leading the medical-scientific strategy of the CVRM therapeutic area, responsible for Hungary medical affairs teams´ development, managing the teams to achieve leadership objectives with a clear patient centric approach, focusing on external scientific partnerships and environment shaping projects, contributing to the clinical development of products and cross-functional collaboration within AstraZeneca.
Key responsibilities :
Leadership, Team Management and People Development
- Build, organize and animate a medical TA team of excellence to ensure the success of the CVRM Therapeutic Area portfolio, building and creating a culture of development and fostering an adequate motivation and working atmosphere
- Supervise direct reports such as Medical Affairs Managers (MAM), Medical Advisors (MA) and / or Medical Science Liaisons (MSL) ensuring integrated and coordinated activities.
- Lead team performance, using managing and developing tools (activity dashboards, performance reviews, coaching, feedback)
- Support team development, focusing on the consolidation of its strengths and the strengthening of improvement areas, ensure implementation of Individual Development Plans, develop skills and scientific leadership of the team
- Support talent management
Strategic & Operational Excellence
Define, lead and implement comprehensive and innovative Medical Plans for the CVRM Therapeutic Area portfolio in alignment with global plans and / or regional guidance (incl. planning and delivery of Evidence Plans)Design and validate objectives, plans and budgets of areas under responsibility.Define and implement External Scientific Excellence projectsDevelop high added-value relationships with external experts, scientific societies and health decision makers of the therapeutic area including future perspectivesProject the image and corporate values of AstraZeneca in internal and external interactionsCross-functional activities
With an entrepreneurial leadership, ensure synergies within Medical Affairs (Global, Europe / CA) and cross-functionality with the transverse teams : Commercial, Market Access, Regulatory Affairs, SM&M, Pharmacovigilance, Medical Information, Medical Evidence and Training.Active contribution to the Value Team Meetings for indications / brands within CVRM TA, including analysis or products in development (pipeline) or existing in the portfolio, identifying their potential future use (new indications, etc.) and business opportunities for the companyActive contribution to development and coordinated of cross-functional Brand Plans for CVRM TAEnsure scientific an clinical input into RWE projects and secure alignment with global medical teamsCompliance
Ensures compliance with AZ code of Ethics, Corporate Governance, Audit requirements and other relevant guidelines, codes, policies and proceduresComplies with all relevant People and SHE standards, policies and processesActs to ensure GCP requirements are fully complied with and in line with the local Quality Management System (QMS) SOP and all other AZ policies and StandardsAs Nominated Signatory (if applicable) ensures that all materials and events are in line with internal SOPs, relevant industry codes and local regulationsEnsures that company confidentiality is maintained ( intellectual property, product information)Personal Development
Continuous development in key areas : Scientific expertise in disease area(s) of company focus; incl. disease state management, AZ products, competitive landscape and emerging therapiesBusiness acumen and strategic thinking; collaborative leadership and management along with advanced strategic thinking within and across field team and TAStrong and effective communication; ability to communicate in a variety of situations with various stakeholdersDate Posted
01-lip-2025
Closing Date