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As one company, we have brought together over 30 brands and leadership positions, expanding and diversifying our product portfolio. Join us in making a remarkable impact on people’s lives around the world. Visit careers.abbvie.com to explore our career opportunities. If you are a current AbbVie or legacy Allergan employee, please visit your intranet site to apply internally.


To apply internally on the AbbVie intranet site please go to myabbvie.abbvienet.com. Next, hover over resources and then select Human Resources. After that, you will select “Global Job Board.” You are now viewing jobs on our internal site.


To apply internally on the Allergan intranet site please go to https://allergan.sharepoint.com/sites/GEP. Select the “AbbVie Jobs” tile under the Tools section.

About AbbVie

AbbVie (NYSE:ABBV) is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world.  For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook or LinkedIn.​

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Associate Medical Director / Scientific Director, Global Medical Affairs - Oncology

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Medical
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2001207 Requisition #
Thanks for your interest in the Associate Medical Director / Scientific Director, Global Medical Affairs - Oncology position. Unfortunately this position has been closed but you can search our 0 open jobs by clicking here.

 Level Commensurate with experience 


Associate Medical Director 
  • Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D. meet requirements) with relevant therapeutic specialty in an academic or hospital environment. Completion of residency and/or fellowship is preferred.
  • National license to practice medicine with relevant therapeutic specialty in an academic or hospital environment. Academic qualification (Dr med or equal) is strongly preferred. Completion of residency and/or fellowship is preferred.
  • Strong experience in oncology/hematology therapeutic area in either pharmaceutical industry, clinical setting or academia, highly preferred
  • Minimal clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent.
  • 1-2 years of experience is preferred.
  • Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in the design of protocols preferred.
  • May possibly have performed protocol design in the academic environment or in the pharmaceutical industry and/or acted as an assistant PI or PI.
  • Interactions normally require the ability to gain cooperation of others, conduct presentations of technical information concerning specific projects/schedules, etc.
  • Ability to interact externally and internally to support global business strategy. Must possess excellent oral and written English communication skills.
  • Ex-Us: At least one further major international language is preferred.

 

Scientific Director 

  • Advanced degree (e.g. PhD, PharmD). Post doctorate experience highly preferred.
  • Ability to provide input and direction to clinical research with appropriate supervision 
  • At least 4 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent
  • Strong experience in oncology/hematology therapeutic area in either pharmaceutical industry, clinical setting or academia, highly preferred
  • Ability to oversee a clinical research program of moderate complexity with minimal supervision
  • Ability to perform and bring out the best in others on a cross-functional global team
  • Ability to interact externally and internally to support a global scientific and business strategy
  • Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols
  • Must possess excellent oral and written English communication skills

Equal Employment Opportunity Employer

At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients.  As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

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