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Daiichi Sankyo
Atlanta, GA, United States
Join a Legacy of Innovation 110 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise a
Job Source: Daiichi SankyoAzurity Pharmaceuticals - US
Atlanta, GA, United States
Direct the activities of US Labeling and Advertising/Promotional Review Teams. Responsible for the oversight of labeling for product registration and commercialization.Ability to provide Advertising/Promotional regulatory insight in line with applicable regulatory guidelines. Serve as a liaison and subject matter expert (SMA) on the interpretation
Job Source: Azurity Pharmaceuticals - USAzurity Pharmaceuticals - US
Atlanta, GA, United States
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad com
Job Source: Azurity Pharmaceuticals - USConfidential
Atlanta, GA, United States
Senior Director, Regulatory Affairs About the Company International labelling organization based in Los Angeles Industry Retail Type Privately Held About the Role The Senior Director, Regulatory Affairs will be responsible for developing and managing labeling for products worldwide as well as overseeing the strategic regulatory leveling HA intera
Job Source: ConfidentialImbria Pharmaceuticals
Atlanta, GA, United States
Company Overview Imbria Pharmaceuticals is a privately held, clinical stage company developing novel therapies for patients with life-altering cardiometabolic disorders. Our clinical programs are focused on restoring or improving the cell’s ability to produce energy in cardiovascular disorders where energetic impairment is a fundamental contributor
Job Source: Imbria PharmaceuticalsImbria Pharmaceuticals
Atlanta, GA, United States
Company Overview Imbria Pharmaceuticals is a privately held, clinical stage company developing novel therapies for patients with life-altering cardiometabolic disorders. Our clinical programs are focused on restoring or improving the cells ability to produce energy in cardiovascular disorders where energetic impairment is a fundamental contributor
Job Source: Imbria PharmaceuticalsArxada
Atlanta, GA, United States
Posted Job Advert Arxada is a global specialty chemicals business that’s committed to solving the world’s toughest preservation challenges through better science. With a proud history of innovation dating back more than a century, we aim to help our customers develop more sustainable solutions that protect and maintain the health and wellbeing of
Job Source: ArxadaPiper Companies
Atlanta, GA, United States
Piper Companies is searching for an Experienced Regulatory Affairs Professional in Advertising & Promotion to lead the neurology regulatory affairs team of a global biopharmaceutical company as Associate Director of Regulatory Affairs (Advertising & Promotion) . The position is a remote opportunity. Responsibilities for the Associate Director
Job Source: Piper CompaniesAtlanta, GA, United States
Executive Director, Regulatory Affairs
About the Company
Pioneering developer & manufacturer of innovative therapeutic medicines
Industry
Biotechnology
Type
Public Company
Founded
1980
Employees
10,001+
Categories
Biotechnology
Biotechnology and Pharmaceuticals
Biotech
Health Care
Pharmaceutical
Pharmaceuticals
Academic Research
Manufacturing
Genomics
Therapeutics
Clinical Care
Patient Management
Healthcare
Life Sciences
Personalized Medicine
Medicine
Chemical Products
Specialties
Biologics
Human therapeutics
and Development of novel products
Business Classifications
B2C
Mobile
About the Role
The Company is seeking an Executive Director of Regulatory Affairs to join their team. This pivotal role involves leading and directing regulatory affairs activities within an assigned therapeutic area, ensuring compliance with global and regional laws and regulations. The successful candidate will provide strategic leadership to the regulatory affairs team, oversee the development of regulatory strategies, and engage in effective interactions with regulatory agencies. Responsibilities also include providing regulatory expertise to commercialization teams, contributing to the development of global and regional product labels, and influencing the regulatory legislative environment in line with the company's policy priorities. The role requires a strong leader with the ability to manage and mentor staff, champion change, and foster a culture of continuous improvement. Candidates for the Executive Director of Regulatory Affairs position at the company should have a Doctorate, Master's, or Bachelor's degree in a relevant field, along with a significant amount of experience in regulatory affairs and at least 6 years of managerial experience. The ideal candidate will have a proven track record of leading teams, excellent communication skills, and the ability to understand and communicate scientific and clinical information effectively. They should be adept at setting organizational direction, anticipating strategic issues, and resolving conflicts to achieve positive outcomes. The role demands a leader who can inspire and empower their team, accelerate progress in line with patient needs, and integrate the company's resources to drive results.
Hiring Manager Title
Senior Vice President Global Regulatory Affairs and Strategy
Travel Percent
Less than 10%
Functions
CEO/President
Non-Profit Management
Operations
General Management
Strategy
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Email Alert for Executive Director, Regulatory Affairs jobs in Atlanta, GA, United States
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