Associate Director, Medical Affairs - Global Biosimilars

Associate Director, Medical Affairs - Global Biosimilars

Teva

Zagreb, Croatia

How you’ll spend your day

• Create expert medical and scientific inputs for biosimilar products and programs;
• Represent the medical function and provide medical inputs to cross-functional teams and global projects related to biosimilars;
• Maintain general scientific expertise, including up-to-date knowledge of international guidelines and requirements for biosimilars;
• Prepare and deliver high-quality internal and external medical and scientific trainings as a subject matter expert, ensuring compliance with current legislation;
• Contribute to the development and approval of promotional and non-promotional materials to ensure optimal use of data, scientific/medical accuracy, and compliance with regulations;
• Provide medical input and consultation during external communication content development;
• Build and maintain relationships with global and regional stakeholders;
• Work in close collaboration within Medical supporting biosimilars to ensure strategic alignment and impactful execution of medical plans;
• Collaborate closely with regional and global biosimilar commercial leads and cross-functional teams (Portfolio, Pipeline, Marketing, Market Access, HEOR, Regulatory Affairs, Pharmacovigilance, R&D);
• Anticipate internal and external business challenges and recommend process, product, or service improvements;
• Contribute to the creation and execution of the functional strategic plan in support of TA and product brand plans;
• Represent the company at major scientific meetings and conferences;
• Lead external expert engagement and insight generation activities;
• Ensure compliance with medical governance and internal policies.

Your experience and qualifications

• Medical degree or PhD with relevant medical experience;
• 8+ years of medical/scientific experience, preferably in a regional or global role;
• Experience in biosimilars (development and launch) would be an advantage;
• Comprehensive understanding of pharmaceutical regulations and compliance frameworks;
• Excellent communication skills and proficiency in English;
• Ability to collaborate effectively in cross-functional, international environments and build strong networks;
• Analytical and strategic thinker with evidence-based decision-making skills;
• Highly organized, self-disciplined, and able to manage priorities and deadlines;
• High integrity, entrepreneurial mindset, and results-driven approach.