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Senior Medical Director (TA)

Date: May 5, 2019

Location: Parsippany, New Jersey, US, 07054

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.  This is how we improve health and enable people to live better, healthier lives.  Join us on our journey of growth!

Job Description

Reporting to the Vice President and Head of NAMA, the incumbent will be responsible for the development of the medical strategy for all respective Teva Respiratory (TR) products’ execution of initiatives in North America.

 

The incumbent will be charged with developing and providing a rigorous scientific and medical foundation for acceptance and usage of Teva Respiratory products. This will be achieved by oversight of the design and implementation of appropriate late Phase studies and post-marketing therapeutic projects and trials.

He/She will also drive the review, decision process and support of investigator initiated trials. 

 

Critical to the success of this organization, the incumbent will need to create positive advocate relationships and partnerships with centers of academic and clinical excellence, national thought leaders, scientific experts and professional organizations in the Respiratory Disease and Allergy-Immunology communities. He/She will also serve as an internal medical strategic lead and partner to the Global MA, Clinical Development, Regulatory, Pharmacovigilance and commercial functions within TR.

 

Qualifications

Scientific Experience -- MD preferred, PhD, PharmD, DO considered, 3+ years of experience in Medical Affairs and/or Clinical Development roles.  

Additional clinical and/or industry experience especially in Respiratory MA preferred. 

Required familiarity with and/or basic experience in the clinical drug development, regulatory processes, designing and conducting clinical trials preferred.

Must be familiar with HEOR as it applies to achieving strategic business goals within his/her scope of work.

 

Function

Medical Affairs

Sub Function

Therapy Area Specialist

Reports To

VP Medical Affairs, NA

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, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.


Nearest Major Market: New York City
Nearest Secondary Market: Newark