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Opportunity: Global Medical Director, Dapagliflozin (#1100084) @ Bristol-Myers Squibb--Princeton, NJ (US)
Submitted by Jody Aikawa; posted on Tuesday, February 08, 2011
RESPONSIBILITIES:
The Global Director dapagliflozin will lead a workstream to supporting evidence generation activities including data gap analyses and a patient registry which help evolve understanding of patient management challenges in diabetes. He/she will input into the Global Thought Leader plan, and provide strategic direction into the Scientific Communication Platform. Additionally, he/she will support the development and commercialization strategy for the Life Cycle program for dapagliflozin, and develop and execute the global medical plan for Life Cycle indications, Demonstrated ability to successfully interact with and provide medical input to influence commercial and clinical development strategy and programs is needed.

REQUIREMENTS:
* The successful candidate will have an advance degree (MD, PhD, or Pharm.D.) with clinical or industry experience.

* 5 or more years of relevant experience in the pharmaceutical industry (medical affairs or clinical development) and broad experience in therapeutic area (diabetes) is preferred.

* The candidate should also have experience working with national and regional physician thought leaders in the area of diabetes, strong analytical skills, an ability to evaluate scientific data and medical literature and extrapolate them to medical, marketing, or sales programs.

* Strong project management skills and ability to work effectively with cross functional teams including clinical, marketing, sales, medical science is needed.

* The individual should be highly organized and motivated with an ability to develop and coordinate multiple projects and initiatives, possessing excellent communication skills, both verbal and written, and strong interpersonal skills and presentation skills.

LOCALE:
Princeton, NJ

HOW TO APPLY:
To apply for this position, copy/paste the following URL into your browser: [link]

DEADLINE:
March 8, 2011

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