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About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healt…
The Regulatory Affairs Manager will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compila…
Job Description: Onsite full time at Princeton Pike. Innovation and Digital Health, Project Manager - Digital Optimization Initiatives Position Summary * The Innovation Lab team…
Job Title: Regulatory & Medical Affairs - Project Manager Job ID: 24-01565 Location: Lawrence Township, NJ, 08648 Duration: 06 Months contract on W2 Onsite full time at Prince…
Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500…
SUMMARY OF POSITION Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and su…
SUMMARY OF POSITION The Sr. Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug developm…
Description Kenvue is currently recruiting for: Regulatory Affairs Manager This position reports to Director, Regulatory Affairs and is based at Skillman, NJ. (Kenvue's corpo…
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here,…
Innova Solutions is immediately hiring for an Global Regulatory CMC Manager Tittle: Global Regulatory CMC Manager Duration: 9 months Contract Location: Lawrenceville ,NJ (onsite…
Responsibilities: Prepare and review CMC submission documents, registration dossiers, health authority briefing packages and responses to health authorities through collaboration…
Responsibilities: Participate in the development of the CMC regulatory strategy for small molecules. These submissions include health authority briefing packages, IND/CTA, NDA, a…
You have reached the maximum number of jobs you can save. To save a new job, please remove one before. Sr. Manager, Global Medical & Regulatory Affairs Management Services New …
SUMMARY OF POSITION Independently authors, compiles, reviews, schedules, and submits high-quality regulatory submissions in adherence with technical document standards that are fu…
SUMMARY OF POSITION The Associate, Regulatory Labeling prepares, reviews and submits to his/her manager high-quality regulatory labeling submissions intended for the FDA within co…
Description Kenvue is currently recruiting for: Project Manager, Self Care This position reports to Senior Manager of the Project Management Office and is based Skillman, NJ …
Join a Market Leader Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative tec…
About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients' lives through the manufacturing and distribution of high-quality pharmaceutic…
SourcePro Search is conducting a search for an experienced Project Manager for our client in the securities trading system environment in Princeton, NJ. This is a hybrid role (2 …