Medical Advisor

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

The Medical Advisor will lead post-marketing clinical research and real-world evidence (RWE) initiatives to optimize product lifecycle management. This role requires integrating scientific expertise with strategic insights to generate robust evidence supporting product safety, efficacy, and value in real-world settings. The candidate will collaborate cross-functionally to drive data-driven decision-making and ensure alignment with regulatory and market needs.

How you’ll spend your day

Post-Marketing Clinical Research & RWE Strategy

• Design and execute post-marketing studies (Phase IV), including protocol development, data analysis, and interpretation of results to address clinical gaps and regulatory requirements.

• Lead real-world evidence projects (e.g., observational studies, database analyses) to evaluate treatment patterns, comparative effectiveness, and long-term outcomes.

• Collaborate with biostatistics and data science teams to apply advanced analytics (e.g., R, SAS) for RWE generation.

Cross-Functional Collaboration

• Partner with Market Access to develop value propositions using RWE for reimbursement and health technology assessments (HTA).

• Support R&D activities as needed.

KOL Engagement & Scientific Communication

• Build and maintain relationships with Key Opinion Leaders (KOLs), facilitating advisory boards and expert panels to gather clinical insights and drive research priorities.

Compliance & Risk Management

• Ensure adherence to GCP, regulatory guidelines (e.g., FDA, NMPA), and internal SOPs in all research activities.

• Monitor and assess safety signals from post-marketing data, collaborating with Pharmacovigilance for risk mitigation.

Your experience and qualifications

• MD, PhD, or master’s degree in clinical medicine, Pharmacology, Epidemiology, or related fields

• 3+ years in pharmaceutical industry roles (Medical Affairs, Clinical Research) with focus on post-marketing studies/RWE

• CNS Disease Experience would be a plus

• Proven track record in study management

• Expertise in real-world data sources (e.g., claims databases, EHRs)

• Strong understanding of regulatory landscapes (e.g., ICH-GCP, RWE guidelines)

• Excellent communication skills in English; proficiency in local language preferred

• Computer literacy: Fluent Microsoft Office operation skills

Make a difference with Teva Pharmaceuticals

Please submit your CV and a cover letter responding to the selection criteria outlining relative keys skills and experience in relation to this role.

Please note that only shortlisted candidates will be contacted.

Reports To

Director, Medical Affairs Greater China

Already Working @TEVA?

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.