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Regulatory affairs Jobs in Rochester, NY
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Regulatory affairs • rochester ny
- Promoted
Senior Director of Regulatory Affairs
VirtualVocationsRochester, New York, United StatesACA Government Affairs Director
ADPUnited States-Home Office, United States-Home Office, NY, USProgram Manager (Regulatory / Risk Management)
Innova SolutionsNew York, NY,New York,United StatesLicensing Coordinator- Regulatory Affairs
Constellation BrandsRochester, New YorkManaging Consultant, Environmental Regulatory FERC Specialist
ERMRochester, New York- Promoted
Physician (Gastroenterology)
Veterans Affairs, Veterans Health AdministrationRochester, NY, United States- oncology pharmacist (from $ 135,200 to $ 487,040 year)
- business development associate (from $ 37,000 to $ 334,880 year)
- informatics nurse (from $ 186,665 to $ 315,680 year)
- genetic counselor (from $ 111,387 to $ 288,960 year)
- data modeler (from $ 97,500 to $ 264,702 year)
- clinical specialist (from $ 78,750 to $ 244,400 year)
- medical social worker (from $ 156,000 to $ 221,296 year)
- healthcare (from $ 56,550 to $ 210,300 year)
- design director (from $ 89,750 to $ 195,000 year)
- Boston, MA (from $ 125,771 to $ 200,600 year)
- Cambridge, MA (from $ 113,100 to $ 200,200 year)
- Atlanta, GA (from $ 87,750 to $ 195,950 year)
- San Francisco, CA (from $ 103,208 to $ 195,773 year)
- San Jose, CA (from $ 104,003 to $ 194,780 year)
- San Diego, CA (from $ 104,546 to $ 193,259 year)
- New York, NY (from $ 90,142 to $ 189,903 year)
- Seattle, WA (from $ 95,000 to $ 185,000 year)
- Pittsburgh, PA (from $ 49,920 to $ 177,310 year)
- Houston, TX (from $ 69,257 to $ 170,000 year)
The average salary range is between $ 74,006 and $ 170,765 year , with the average salary hovering around $ 105,135 year .
Related searches
Senior Director of Regulatory Affairs
VirtualVocationsRochester, New York, United States- Full-time
A company is looking for a Senior Director, Drug Development & Regulatory Strategy. Key Responsibilities Oversee regulatory strategy, execution, and compliance for early-stage drug development Lead a team of Regulatory Affairs professionals and serve as a liaison with global health authorities Define regulatory strategy plans and manage regulatory submissions and interactions with regulatory agencies Required Qualifications PhD in a related discipline preferred 10 years of experience in regulatory affairs in a CRO, biotechnology, or pharmaceutical setting Demonstrated success in leading early-stage regulatory strategy and submissions in North America Deep knowledge of Health Canada and FDA regulatory frameworks Understanding of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP)