As part of Teva’s Medical Affairs EU team, you will be responsible to:
Prepare, review and oversee medical and scientific inputs within Teva and externally, including but not limited to: medical assessments, expert reports/overviews, briefing documents for scientific advice, orphan designations;
Review and approve promotional and non-promotional materials, educational and training materials for marketed and branded generics;
Review company initiated phase IV studies & Investigator Sponsored Studies (ISS) for generics in EU;
Identify applications of functional knowledge and existing methodologies to solve complex problems;
Anticipate internal and/or external business challenges and/or regulatory issues; recommends process, product or service improvements;
Establish and maintain effective relationships within Medical Affairs, other organizational units and cross-functional teams in the company;
Represent medical function and provide medical inputs to other EU regional functions, including but not limited to: Marketing, Regulatory Affairs, Commercial, Portfolio/Pipeline, R&D, Legal/Intellectual Property, Pharmacovigilance.
Medical Degree (strongly preferred) or PhD with relevant medical experience;
10 years of relevant medical/scientific experience; candidates with less experience will be also considered;
Ability to liaise with different internal stakeholders;
High level of personal integrity, cause and effect thinking along with the ability to innovate;
Teamwork - comfortable working in cross-functional teams;
Fluency in English with strong communication skills and ability to liaise with different internal and external stakeholders.