A company is looking for a Senior Manager, Regulatory Affairs.Key Responsibilities : Lead creation and maintenance of Company Core Data Sheets (CCDS) activitiesDrive global implementation of CCDS into country-specific labelingFormulate and drive global technology initiatives for labeling and content managementRequired Qualifications : Bachelor's degree in a scientific discipline, with a preference for Masters or PhDMinimum of 7 years of RA experience, including 2 years of CCDS experienceAbility to work effectively in a multinational environmentExpert regulatory knowledge and sound scientific basisAbility to oversee multiple projects in a matrix team environment
Sr Manager Regulatory Affairs
A company is looking for a Senior Manager, Regulatory Affairs. Key Responsibilities:Lead creation and maintenance of Company Core Data Sheets (CCDS) activitiesDrive global implementation of CCDS into country-specific labelingFormulate and drive global technology initiatives for labeling and content ...
Project Manager, SECURE Southeast - Research Compliance & Regulatory Affairs
Discover Your Career at Emory University:.Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future.We welcome candidates who can contribute to the diversity and excellence of our academic community....
Regulatory Affairs Manager
Key Responsibilities:Provide strategic and tactical regulatory guidance for in vitro diagnostics/companion diagnosticsDevelop regulatory strategies for product registration and study designsInteract with diagnostic partners and regulatory agencies for submissions and meetingsRequired Qualifications:...
Regulatory Affairs Manager
The Product Safety & Regulatory Compliance Team is seeking a Regulatory Affairs Manager to join our team. Experience working in regulatory compliance, chemical control, regulatory affairs, environmental, laboratory or product safety in the agriculture industry. The Product Safety & Regulatory Compli...
Regional Manager, Regulatory Affairs & Quality - Medical Device Americas Region
Symmetrio is currently recruiting a qualified individual to fill the role of Regional Manager Regulatory Affairs & Quality Americas for our client, a global medical device company. Act as the Regional Coordinator for regulatory submissions and regulatory strategies in the Americas. Regulatory Af...
Regulatory Writing Sr Manager (Biologics)
Need experience briefing documents with Significant Clinical Content/Module 2 Clinical Summary Documents (Looking for 3-4 years of experience with these document types).Need people with leading writing activities for Drugs/Biologics.Biotech/Pharmaceutical industry....
Sr. Business Affairs Manager
Business Affairs Manager is a leader and supportive team player on the Production Team responsible for managing Business Affairs functions and talent aspects for various Razorfish Content Productions (TV/Radio/Print/Video/ Social/Influencer etc. Work closely with Business Affairs Team to maintain Ri...
Manager Scientific and Regulatory Affairs Compliance and Innovation
Enable growth as a Scientific and Regulatory Affairs (SRA) business partner for innovation projects, represent SRA function in charters, and act as SRA interface with innovation teams. The successful candidate should be passionate about always seeking synergies and demonstrate their ability to drive...
Senior Program Manager, Regulatory Affairs - Labeling (REMOTE).
Demonstrated successful leadership experience, including in multi-functional teams including Global Sales & Marketing (GSM), Regulatory, Legal, Clinical/Medical Affairs, Quality, Corporate Communications, and other Functional Departments. Advanced experience with regulatory review of labeling · Expe...
Manager, Japan Regulatory Affairs Strategy, Devices
Holds responsibility for medical device(s) and supports the Global Regulatory Lead (GRL)/ in the development & execution of the regulatory strategy. In cooperation with Global Device Regulatory team, leads activities to develop and implement regulatory strategies to secure global medical device lice...