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Medical Advisor

3+ years
Not Disclosed
10 June 4, 2025
Job Description
Job Type: Full Time Education: MD, PhD, or Master’s Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Medical Advisor

Date Posted: May 13, 2025
Location: Shanghai Shi, China, 200040
Company: Teva Pharmaceuticals
Job ID: 61533


Who We Are

At Teva, we are committed to improving global health by making quality medicines accessible to millions. As the world’s largest producer of generic medicines and a key contributor to the World Health Organization’s Essential Medicines List, we serve over 200 million people each day. With operations in nearly 60 countries, we’re constantly expanding our impact—and looking for passionate individuals to join us in shaping a healthier future.


The Opportunity

As a Medical Advisor, you will lead post-marketing clinical research and real-world evidence (RWE) strategies that support the lifecycle of Teva products. You’ll play a key role in generating data that enhances our understanding of safety, efficacy, and cost-effectiveness in real-world settings. This position requires strong collaboration across departments, scientific rigor, and the ability to engage with key opinion leaders.


How You’ll Spend Your Day

Post-Marketing Research & RWE Generation:

  • Lead the design and execution of Phase IV clinical trials and observational studies.

  • Manage all aspects of post-marketing research including protocol development, data analysis, and results interpretation.

  • Apply RWE methodologies (e.g., use of EHRs, claims databases) to evaluate real-world outcomes, treatment adherence, and cost-effectiveness.

  • Partner with biostatistics and data science teams using tools like R or SAS for analysis.

Cross-Functional Collaboration:

  • Work closely with Market Access teams to build RWE-based value propositions for HTA and reimbursement.

  • Collaborate with R&D and regulatory affairs to support data submissions and lifecycle initiatives.

Stakeholder Engagement & Scientific Communication:

  • Establish and maintain relationships with KOLs and clinical experts.

  • Organize and lead advisory boards, expert panels, and other engagement platforms.

  • Contribute to the development of scientific publications, abstracts, and presentations.

Compliance & Safety:

  • Ensure all studies comply with GCP, ICH, FDA, and NMPA guidelines and Teva SOPs.

  • Collaborate with Pharmacovigilance to identify and address post-marketing safety signals.


Your Experience and Qualifications

Required:

  • Advanced degree: MD, PhD, or Master’s in Clinical Medicine, Pharmacology, Epidemiology, or related discipline.

  • 3+ years of experience in the pharmaceutical industry in Medical Affairs or Clinical Research, with a focus on post-marketing studies or RWE.

  • Hands-on experience with real-world data (e.g., EHRs, insurance claims databases).

  • Familiarity with regulatory frameworks and global clinical practice guidelines.

Preferred:

  • Therapeutic experience in CNS disorders is a strong advantage.

  • Proficiency in English is required; Mandarin Chinese is highly preferred.

  • Strong skills in Microsoft Office and relevant statistical or data analytics software.


Reporting Line

Reports To: Director, Medical Affairs Greater China