- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Medical Director is responsible for supporting the Product Safety Leads (PST) and ... the authorship of key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans… more
- AbbVie (North Chicago, IL)
- …integrity, fosters regulatory compliance, and contributes to the overall success of drug/ device development programs. Director , Medical Affairs Quality ... information and other regulatory commitments., covering the AbbVie drug, device and cosmetic portfolio. The role drives quality excellence...MA in scope. The role reports to the Senior Director of Safety , Vigilance and Medical… more
- AbbVie (North Chicago, IL)
- …systematically defines quality objectives, both strategic and applicable regulatory requirements. Director , Safety , Regulatory and Medical Affairs Quality ... quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfolio. The role oversees generation and...assurance excellence mindset. The role reports to the Senior Director of Safety , Vigilance and Medical… more
- AbbVie (North Chicago, IL)
- …safety database and search strategy, construction/maintenance) and Global Pharmacovigilance Medical Device functionality (coordination of processing and US ... medical terminology coding quality in ...reporting of stand-alone medical device and combination product incident reports)....reporting of stand-alone medical device and combination product incident reports). . Proactively identifies,… more
- AbbVie (North Chicago, IL)
- …set the strategy for key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans + ... Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product Safety Teams (PST) and supports one or more psychiatry products… more
- AbbVie (North Chicago, IL)
- …appropriate write the key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses, 15 day aggregate reports. ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...safety surveillance for pharmaceutical / biological / drug - device combined early oncology products + Lead, set the… more
- AbbVie (North Chicago, IL)
- …the strategy for key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Facebook, Instagram, YouTube and LinkedIn. Job Description The Product Safety Team (PST) lead for late stage oncology products,… more
- AbbVie (North Chicago, IL)
- …appropriate write the key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses, 15 day aggregate reports. ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...safety surveillance for pharmaceutical / biological / drug - device combined products + Lead, set the strategy and… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... line functions. Partners with Clinical, Regulatory, Operations, Quality, Pre-clinical Safety , and Commercial organizations. Apprises CMC Management of strategies,… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... line functions. Partners with Clinical, Regulatory, Operations, Quality, Preclinical Safety and Commercial Organizations. Apprises CMC Management of strategies,… more
- AbbVie (North Chicago, IL)
- …the AbbVie drug, device and cosmetic portfolio. The role reports to a Director of Safety , Vigilance and Medical Affairs Quality Assurance. There is ... that includes expert guidance to enable successful inspections with safety , RA and MA topics in scope. + Is...(at least 8 years) with sufficient exposure to pharmaceutical, medical device , or combination product related industries.… more