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Associate Director, Medical Affairs - Global Biosimilars

Teva

Zagreb, Croatia
Pharmaceutique
Publié le 13 novembre 2026

Description du poste

Associate Director, Medical Affairs - Global Biosimilars Teva Zagreb, Croatia Our Team, Your Impact A strategic opportunity for an experienced medical professional to provide expert medical and scientific input for biosimilar products and programs across global and regional teams. You will represent the medical function in cross-functional teams and global projects, build relationships with global and regional stakeholders, and contribute to the functional strategic plan supporting TA and product brand plans. The role offers visibility at major scientific meetings and conferences and the chance to lead external expert engagement and insight generation. How You ll Spend Your Day Create expert medical and scientific inputs for biosimilar products and programs; Represent Medical in global biosimilar projects and cross-functional teams (Portfolio, Pipeline, Marketing, Market Access, HEOR, Regulatory Affairs, Pharmacovigilance, R&D) and with commercial leads; Maintain up-to-date knowledge of international guidelines and requirements for biosimilars; Deliver internal and external scientific trainings as a subject matter expert, in line with legislation; Contribute to development and approval of promotional and non-promotional materials for accuracy and compliance; provide medical input to external communications; Build relationships with global and regional stakeholders; align closely within Medical on medical plans; Anticipate business challenges and recommend process, product or service improvements; Contribute to the functional strategic plan in support of TA and product brand plans; Represent the company at major scientific meetings; lead external expert engagement and insights; Ensure compliance with medical governance and internal policies. Your Skills and Experience Medical degree or PhD with relevant medical experience; 8+ years of medical/scientific experience; Experience in biosimilars (development and launch); Comprehensive understanding of pharmaceutical regulations and compliance frameworks; Excellent communication skills and proficiency in English; 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, able to manage priorities and deadlines; High integrity, entrepreneurial mindset and results-driven approach. Also Good to Have Medical/scientific experience in a regional or global role. Apply Now