Regulatory Affairs: Average Salary in Lawrenceville, GA in 2024
Find out what the average Regulatory Affairs salary is in Lawrenceville, GA
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Global Regulatory Affairs Specialist
A company is looking for a Global Regulatory Affairs Specialist. ...
Strategy Director, Global Regulatory Affairs
Demonstrated ability to drive high-level regulatory strategy and navigate complex regulatory landscapes. The client is seeking a highly experienced professional to lead their regulatory strategy for a late-phase oncology program. Spearhead regulatory submissions for the oncology portfolio, driving s...
Regulatory Affairs Specialist - Contract
Key Responsibilities:Plan, coordinate, and drive the development and evaluation of regulatory strategies and submissionsManage resources and provide regulatory leadership and mentoringConduct quality audits, develop management systems, and represent projects at various meetingsRequired Qualification...
Associate Director, US Regulatory Affairs Strategy
Support the lead regulatory strategy for late-phase oncology programs, ensuring alignment with global regulatory requirements. Minimum of 8 years of industry experience, with at least 4 years in regulatory affairs. Strong technical proficiency in regulatory affairs is crucial. The client is seeking ...
Senior Director Global Regulatory Affairs
Postgraduate degree in Regulatory Affairs preferredMinimum 10+ years of regulatory experience in biotech or pharmaceutical industryPrevious oncology experience highly preferredMinimum of 7 years regulatory experience in drug development and approval process. Key Responsibilities:Develop and implemen...
Strategy Director, US Regulatory Affairs
Minimum of 10 years in the industry, with at least 8 years dedicated to regulatory affairs. Demonstrated ability to drive high-level regulatory strategy and navigate complex regulatory landscapes. The client is seeking a seasoned professional to lead their regulatory strategy for a late-phase oncolo...
Regulatory Affairs Manager
Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager. Work with CMC cross-functional teams and Regulatory Affairs teams. CMC regulatory experience, Sterile Injectable experience preferred. Participate in the development of the CMC regulatory strategy for post-approval small molecule...
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...
Quality Assurance / ISO Specialist (ISO 15189)
IBEX IT Business Experts, LLC is seeking a Quality Assurance/ ISO Specialist (ISO 15189) who exhibits professional knowledge of the concepts, theories, principles and practices of medical technology sufficient to develop and maintain a quality assurance/control program for the JPC's Molecular Labora...
Senior Associate Regulatory Compliance
A company is looking for a Senior Associate, Regulatory Compliance (Credit Card). ...
Regulatory Specialist US
A company is looking for a Regulatory Specialist in the US. ...
Clinical Value Analysis Program Manager
A company is looking for a Clinical Value Analysis Program Manager (Nursing). ...
Senior Quality Assurance Specialist
A company is looking for a Senior Quality Assurance Specialist. ...
Program Manager and Analyst
A company is looking for a Program Manager and Analyst. Key Responsibilities:Conduct organizational studies and evaluations, design systems and procedures, and prepare operations manualsPerform quantitative analyses of information affecting investment programsAnalyze budget estimates for completenes...
Sr Technical Writer
A company is looking for a Senior Technical Writer. ...
Payroll Compliance Specialist
A company is looking for a Payroll Compliance Documentation Specialist. ...
Technical Writer IT Documentation Specialist
A company is looking for a Technical Writer. ...
Associate Regulatory Affairs-CMC
A company is looking for an Associate Regulatory Affairs-CMC. ...
Technical Writer Remote WV
Key Responsibilities:Creating and maintaining electronic files for documentation and contact managementTracking workflow of multiple tasks and maintaining task statusCollaborating with underwriters and brokers for pre-bind and post-bind activitiesRequired Qualifications:Four or more years of experie...
Compliance Specialist - Remote
A company is looking for a Compliance Specialist - Remote (US). ...
Remote PBM Pharmacist
A company is looking for a Remote PBM Pharmacist. ...
Principal Compliance Analyst
A company is looking for a Principal Compliance Analyst for a remote position. ...
Associate Director Regulatory Affairs
A company is looking for an Associate Director, Regulatory Affairs. ...
Clinical Pharmacist Reviewer - Remote
A company is looking for a Clinical Pharmacist Reviewer for a remote position. ...
Supply Chain Project Manager
A company is looking for a Supply Chain Project Manager. ...