Regulatory affairs associate jobs in Raleigh, NC

years Pharmaceutical R&D experience with Regulatory Submission experience. The person should be.. Must have pharmaceutical development experience and experience and have worked in a regulatory role..

Senior Director, Regulatory Affairs The Company. Our mission is to improve the health and quality of.. The Opportunity. Verona Pharma is currently recruiting a Senior Director, Regulatory Affairs to join our..

Mantell Associates is partnered with a biopharmaceutical company that's bringing innovative change to.. Director Senior Director of Regulatory Affairs. Responsibilities. Serve as a thought leader on..

Job Description Job TitleRegulatory Affairs SpecialistCollaborate with Innovative 3Mers Around the.. Here, you will make an impact by Leading product teams for regulatory product certification expertise..

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..

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..

I.e., participates in and manage core team relationships or represent GRT to TAM or XRC etc Experience RequiredAt least ten years of experience within Regulatory Affairs of which at least five..

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..

We are currently seeking a Regulatory Compliance Manager to join our team. This position will lead the.. Train others on regulatory matters. Perform all regulatory reporting and filing as required by internal..

The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and.. The Senior Regulatory Specialist responsible for Canadian legislation provides subject matter expertise..

Professionals around the globe expertly provides customizable solutions for their clients' risk, portfolio management, middle office, investor relations, accounting, regulatory, compliance, and..

This position leads Regulatory Reporting initiatives that improve data quality, governance, and.. Reviews feedback from associates in order to identify areas of improvement within data management..

Build testing to ensure data integrity and accuracy of the data in all internal and external reporting processes. 9. Prepare additional data for audit purposes and or other regulatory reports..

You will partner closely with the global representatives of the various Technology Services functional areas, GOTO regional regulatory contacts, and Regulatory Affairs in addressing requests..

Responsibilities The Senior Regulatory Specialist responsible for Canadian legislation identifies.. The Senior Regulatory Specialist responsible for Canadian legislation provides subject matter expertise..

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..