Latest Regulatory Affairs Pharmaceutical jobs in Lake Forest, IL

10 Regulatory Affairs Pharmaceutical Jobs in Lake Forest, IL

Clinical Project Manager Randstad Life Sciences US - Lake Forest, IL, United States cross-collaboration amongst functions involved in product launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time 14 days ago
clinical project manager iii (non-md) Randstad - lake forest, illinois involved in product launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time pharmaceutical industry or consulting experience $90 - $104.42 per hour 17 days ago
HEOR Project Manager----Remote US Tech Solutions - North Chicago, IL, United States launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time pharmaceutical industry or consulting experience in HEOR required 14 days ago
Clinical Project Manager III (HEOR) US Tech Solutions, Inc. - Mettawa, Illinois launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). • Minimum 5+ years of full-time pharmaceutical industry or consulting experience in HEOR required 2 days ago
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Clinical Project Manager III (Non-MD) Mindlance - Mettawa, Illinois , regulatory, etc.). • Minimum 5+ years of full-time pharmaceutical industry or consulting experience in HEOR required. • Experience in immunology is a plus. What are the top 3-5 skills, experience or education 2 days ago
Senior Scientific Director, International Medical Affairs- Oncology Mettawa, IL stakeholders (e.g., commercial, clinical operations, market access, regulatory) as they relate to on-going medical affairs projects. Experience of leading successful teams in pharmaceutical medicine. Experience 10 days ago
Scientific/Medical Director, Medical Affairs - Gastro Pipeline Mettawa, IL in Medical Affairs with Global Medical Affairs experience highly preferred. Minimum of 4 years of clinical trials direct management experience in the pharmaceutical industry or academia or equivalent. 4+ years 17 days ago
Sr. Regulatory Affairs Specialist - Hybrid (IV Solutions) Baxter - Round Lake, IL or lead Regulatory Affairs in small project teams What do you bring Bachelor's degree or country equivalent in a scientific field Minimum of 2 years regulatory or equivalent experience within 25 days ago
Senior Manager, Medical Affairs Quality ( On-site, IL based) North Chicago, IL in the pharmaceutical, medical device/nutritional or related industry. Four years in compliance/auditing or regulatory affairs is desirable. Total combined experience expected to be at least 10 years. ASQ certification 30 days ago
Scientific Director, US Medical Affairs - Dermatology Mettawa, IL required. 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred. Minimum of 4 years of clinical trials direct management experience in the pharmaceutical 30 days ago

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