- AbbVie (North Chicago, IL)
- …Description Conceives, executes and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve ... study proposals and leads those efforts. Anticipates and critically evaluates Clinical Pharmacology , PK/PD or regulatory advances, strengths, weaknesses,… more
- AbbVie (North Chicago, IL)
- …leads those efforts. Anticipates and critically evaluates Statistical, PK/PD, Clinical Pharmacology , or regulatory advances, strengths, weaknesses, opportunities ... for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: + Executes… more
- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Director in CMC Statistics is responsible for providing statistical ... is determined by years of experience, education, and relevant experience. Qualifications for Associate Director , Statistics (CMC): + MS (with 10+ years of… more
- AbbVie (North Chicago, IL)
- …+ Understand and apply concepts in mechanisms of action in immunology, pharmacology , and non- clinical toxicology to inform safety surveillance and mitigation ... assets, the AMD will collaborate with the Group Medical Director to develop of best practices in patient safety...measures in clinical trials. + Maintain knowledge of applicable regulations and… more
- AbbVie (North Chicago, IL)
- …impactful rotational assignments within core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs, ... Regulatory Affairs, and Clinical Development (both early and late stage.) In addition...site personnel, and AbbVie study staff. + Help oversee clinical studies, supporting the monitoring of overall study integrity,… more
- AbbVie (North Chicago, IL)
- …for a product(s) within a Therapeutic Area and supports the Manager (Senior Manager, Associate Director , Director (Global Regulatory Lead (GRL)), in the ... to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial. Functions independently… more