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Astellas Pharma US, Inc.
Associate Medical Director/Medical Director, Medical Affairs,
Location: Deerfield,
Illinois
00000
Posted on:
8/21/2009 8:26:21 AM
Postion type:
Full time
Job Code:
419115
Required Education:
Salary:
DESCRIPTION
Astellas is the bright spot in the pharmaceutical industry – not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomorrow, Astellas is the place where you can shine. We offer a different kind of work culture. A high standard of ethics is mandatory. Quality is our pledge. Diversity is valued. Individual initiative is rewarded. Astellas offers an environment where our employees can make a real difference. Come, shine with us!The Associate Medical Director/Medical Director, Medical Affairs position will be responsible for: the development of P3b/P4 studies and medical monitoring for SL studies; enhancing scientific relationships with key opinion leaders; reviewing promotional and educational material for accuracy; leading consultant and advisory meetings; and reviewing grant applications for scientific merit. Responsibilities will also include ensuring strategic alignment among functional groups within Medical Affairs; regular interactions with senior product and clinical management for strategic development issues and marketing operations; and contributing to life-cycle management. This person will contribute as a medical director to product specific and therapeutic area functions such as publications, medical information, medical education, and consultancy and advisory boards. This person will be responsible for development of post-marketing clinical development plans including design of P3B, P4 studies. They will assist the commercial team in development and communication of consistent global and regional brand messaging across indications. They will provide technical scientific/medical consultation to the commercial team to ensure accuracy and compliance with Astellas standards. They will help to develop phase IIIb/IV clinical trial needs and strategies to support brand. They will assist in the development and execution of brand publication strategies. Effective performance of activities requires minimal supervision or guidance by the Vice-President of Medical Affairs.
REQUIREMENTS:
M.D. degree, Board Certified or Board Eligible in Designated Specialty (preferred) with subject matter expertise in dermatology or ImmunologyThree years clinical or clinical research experience preferredOne year experience in the pharmaceutical industry preferredExcellent communication and presentation skills, strong interpersonal skills.Strong clinical research/medical affairs background, and excellent problem solving abilities.Demonstrate abilities to work effectively in a team environment.Ability to interpret and evaluate clinical data. Leadership skills and ability to effectively manage projects and timelines. Knowledge of pharmaceutical clinical development and ability to effectively apply technical principles, theories, and concepts to clinical drug development. Knowledge of FDA, other regulatory agency and professional requirements, regulations and guidancesAble to work independently on all aspects of assigned projectsExcellent organizational skills
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