Regulatory affairs associate jobs in Raleigh, NC

Key Responsibilities. Develop and implement regulatory labelling strategies for new product labels and.. Candidate Requirements. Associate Director Level. Minimum of 7 years in the pharmaceutical industry..

The Regulatory Affairs Specialist will assist or lead a variety of regulatory tasks in support of global.. In this role, you will. Perform regulatory assessments for product changes including regulatory..

IAmMerz Are you ready to galvanize a team around a culture of care, putting patients first to spark change? The Regulatory Affairs Specialist coordinates the regulatory activities for life cycle..

Job Description Job Description Senior Director, Regulatory Affairs The Company. Our mission is to.. The Opportunity. Verona Pharma is currently recruiting a Senior Director, Regulatory Affairs to join our..

For additional information, please visit. Position Overview The Director, Regulatory Affairs is.. The position is also responsible for oversight and execution of global regulatory strategies and..

Prepare briefing materials for UBS senior management in advance of regulatory meetings. drive the.. coordinate with other Regulatory Affairs teams, including submitting relevant US updates for global..

Biotechnology Scientific secondary school diploma with at least 10 years of experience within International Regulatory Affairs Chiesi USA is an equal opportunity employer committed to hiring a..

The Regulatory Affairs Specialist coordinates the regulatory activities for life cycle management of.. This includes assisting with regulatory timelines as well as coordination of submissions to FDA and..

Hybrid work schedule. minimum 3 days a week in Raleigh office Responsibilities Advisory support and coverage for Regulatory Relations, Regulatory Affairs, Risk Management (1st and 2nd Line..

Associate) Director, US Regulatory Affairs, Advertising & Promotion. Permanent. MA, NC, GA Proclinical.. The (Associate) Director, US Regulatory Affairs, Advertising & Promotion will. Provide regulatory..

A solid scientific background. Ph.D., MD, PharmD, MS, or BS. 10 years or more experience in the pharmaceutical industry, with significant experience in Regulatory Affairs and related non..

BiotechnologyScientific secondary school diploma with at least 10 years of experience within International Regulatory AffairsChiesi USA is an equal opportunity employer committed to hiring a..

Director of Global Regulatory Affairs Class III. Structural Heart. PMA Santa Clara. Hybrid Remote Full.. Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st..

A solid scientific background. Ph.D., MD, PharmD, MS, or BS. 10 years or more experience in the pharmaceutical industry, with significant experience in Regulatory Affairs and related non..

The Regulatory Affairs Senior Specialist. Medical Devices coordinates the regulatory activities for.. This includes assisting with regulatory strategies and timelines as well as the development and..

Job Purpose. The Chiesi. Regulatory Affairs internship will be an immersive experience that will include.. Summary of Key Responsibilities. 80. Global Regulatory Affairs Project Coordination. Coordinating..

Description Reporting to the Vice President of Global Regulatory Affairs (GRA), the Director of Chemical.. You will lead a global team of regulatory professionals to establish business strategies providing..

Job Description Job Description As a member of the Regulatory Engineering Team, you will be responsible.. OnLogic's regulatory team is extremely forward thinking in its methods and truly an asset to the..

McGuireWoods Consulting is a leader in developing innovative and strategic ways to serve our clients. Founded in 1998 as a full service public affairs firm, our consultants provide federal..