- AbbVie (Mettawa, IL)
- …7. Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of ... based in Irvine, CA The Senior Director, Pipeline Medical Strategy Lead provides specialist medical and scientific...pharmaceutical industry or equivalent. Minimum of 10 years of clinical trial or medical affairs experience in… more
- AbbVie (Mettawa, IL)
- …knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of ... different products. + Participation in design and execution of clinical trial safety, product safety and risk...to interact externally and internally to support global business strategy . Ability to run a complex clinical … more
- AbbVie (Mettawa, IL)
- …and supports training on MI materials. + Participation in design and execution of clinical trial safety, product safety and risk management plans. + Mentors and ... Instagram, YouTube and LinkedIn. Job Description Primary Job Function: + Provides specialist medical and scientific strategic and operational input into core medical… more
- AbbVie (Mettawa, IL)
- …or equivalent. 4+ years of experience is preferred. + Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements ... Job Description The Scientific Director, Medical Affairs- Dermatology provides specialist medical and scientific strategic and operational input into...governing clinical trials and experience in development strategy … more
- AbbVie (Mettawa, IL)
- …industry or academia or equivalent is preferred. + Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements ... Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical/scientific strategic and operational input into core medical...governing clinical trials and experience in development strategy … more
- Randstad US (Chicago, IL)
- …example, orphan drug applications, Health Authority advice (EMA and FDA), paediatric plans, clinical trial designs and HA feedback. The assessment will include ... work hours: 9 to 5 education: Bachelors responsibilities: The Regulatory Affairs Specialist will be the regulatory representative for assigned due diligences, under… more