Latest Clinical Risk Management jobs in Mettawa, IL

31 Clinical Risk Management Jobs in Mettawa, IL

Senior Scientific Director, International Medical Affairs- Oncology Mettawa, IL , product safety and risk management plans. Mentors and leads a team of medical affairs professionals Qualifications Relevant scientific, medical or pharmacy background with postgraduate qualification 7 days ago
Medical Director, Medical Affairs- Dermatology Mettawa, IL , design of affiliate/Area/Global protocols and their reports across different products. Participation in design and execution of clinical trial safety, product safety and risk management plans. May 12 days ago
Scientific/Medical Director, Medical Affairs - Gastro Pipeline AbbVie - Mettawa, Illinois , scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities. Participation in design and execution of clinical trial safety, product safety and risk 15 days ago
Assistant/Associate Scientific Director, US Medical Affairs- Oncology AbbVie - Mettawa, IL communication content and supports training on Medical Information (MI) materials. Participates in design and execution of clinical trial safety, product safety and risk management plans. Track RMP implementation 20 days ago
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Scientific/Medical Director, Medical Affairs - Gastro Pipeline Mettawa, IL to the regulatory authorities. Participation in design and execution of clinical trial safety, product safety and risk management plans. May also carry responsibility for routine and ad hoc safety monitoring reports 14 days ago
Clinical Project Manager Randstad Life Sciences US - North Chicago, IL, United States timely availability of clinical supplies. Responsible for protocol specific clinical supplies scenario analysis, risk management and contingency planning. Forecasts protocol specific bulk drug product 11 days ago
Senior Scientific Director, International Medical Affairs- Oncology Mettawa, IL , product safety and risk management plans. Mentors and leads a team of medical affairs professionals Qualifications Relevant scientific, medical or pharmacy background with postgraduate qualification More than 30 days ago
Clinical Coordinator Randstad Life Sciences US - North Chicago, IL, United States regulations. Identifies, develops, communicates and tracks project timelines, activities, logistics, and milestones. Responsible for protocol specific clinical supplies scenario analysis, risk management 14 days ago
Clinical Project Manager I / II------North Chicago, IL / Hybrid US Tech Solutions - North Chicago, IL, United States for protocol specific clinical supplies scenario analysis, risk management and contingency planning. Forecasts protocol specific bulk drug product requirements , including comparator agents, ancillary supplies 14 days ago
GxP Consultant Zifo Technologies Inc. - Deerfield, IL, US (GLP), 210 and 211 (GMP), and 820 (Quality System Regulations). Experience with risk management techniques such as FMEA, 5 WHYs or similar. Office Productivity Tools: MS Project, VISIO, Word, Excel 8 days ago

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