Associate Medical Director

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

The opportunity

Reporting to the Senior Medical Director, North America Medical Affairs (NAMA), the Associate Medical Director – Biosimilars is responsible for executing the medical strategy that supports Teva’s biosimilar portfolio across North America. The role provides the scientific and clinical foundation required to drive the understanding, appropriate adoption, and value recognition of Teva’s biosimilar products. The incumbent will cultivate and maintain strong, strategic relationships with national and regional opinion leaders, centers of excellence, and key professional organizations within the oncology immunology and broader biosimilars communities.

This position collaborates closely with internal partners—Commercial, HEOR, Scientific Communications, Medical Education, Medical Information, and Patient Advocacy to ensure aligned, evidence‑based strategies that support the successful development, launch, and lifecycle management of biosimilar products.

How you’ll spend your day

Medical Strategy & Scientific Leadership 

• Contribute to the development and execution of the medical strategy for Teva’s biosimilar portfolio, ensuring alignment with therapeutic area and brand objectives.
• Support the annual medical operating plan, including identification of evidence gaps, Phase IV needs, real‑world evidence opportunities, and collaborative clinical studies.
• Participate in the evaluation and refinement of clinical study concepts, proposals, and protocols; work closely with R&D, Operations, and HEOR to ensure scientific rigor and clinical relevance.
• Collaborate with Medical Affairs colleagues to develop high‑quality scientific and educational materials for congresses, field medical engagement, and strategic communications.
• Provide medical and clinical trial support for corporate‑sponsored and investigator‑initiated studies.
• Serve as a core scientific resource to U.S. Field Medical teams (MSL/MOL), Scientific Communications, Publications, Regulatory, Business Development, Training, Medical Information, and Commercial partners.
• Under guidance of the Senior Medical Director, lead and manage assigned medical projects, ensuring delivery of scientifically accurate and strategically aligned medical insights and recommendations.
• Co‑lead the agenda design, content development, and execution of Medical Advisory Boards for biosimilar products and indications.
• Ensure scientific accuracy and integrity across publications and congress materials, including review of abstracts, posters, manuscripts, and symposia content.
• Build and maintain strong relationships with key opinion leaders, academic institutions, clinical experts, and professional societies in oncology and immunology biosimilars.
• Act as a medical expert supporting biosimilar launch readiness, labeling comprehension, data interpretation, and disease‑state education.

National Field Expert Engagement 

• Establish, nurture, and manage scientifically credible relationships with national and regional thought leaders in biosimilars, oncology, and autoimmune therapeutic areas.
• Conduct balanced, compliant scientific exchanges that advance understanding of biosimilar science, interchangeability principles, clinical data, and real‑world evidence.
• Serve as a medical and scientific resource to healthcare professionals and internal stakeholders by responding to unsolicited medical information requests, delivering medical education, and supporting congress activities and advisory boards.
• Attend and contribute to major medical congresses, investigator meetings, and relevant internal scientific events.
• Collect, analyze, and communicate medical insights and competitive intelligence relevant to biosimilars and therapeutic areas of interest, informing strategic decision‑making across Medical Affairs and cross‑functional teams.

Your experience and qualifications

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered. 

• Advanced degree required: PhD, PharmD, DO, or MD.
• A minimum of 3 years of experience in Medical Affairs and/or C