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SSA-150-Adverse-Events

Associate Director, Global Trial Management (1 of 2 positions Titusville, NJ)

To learn more about opportunities with the Johnson & Johnson Family of Companies, visit us ...

Associate Scientist

Associate Scientist needed for a 6-month contract. Responsibilities include, but are not limited to,...

Document Management System Business Administrator

Kyowa Pharmaceutical Inc. (KPI) located in Princeton, New Jersey, is part of a Tokyo-based, $3 ...

Associate Director, Advertising & Promotion

To learn more about opportunities with the Johnson & Johnson Family of Companies, visit us ...

CMC Regulatory Manager - Clinical Research - Central NJ - 4 month opportunity!

Kelly Clinical Resources is seeking a CMC Contract Regulatory Manager to assist with NDA Annual R...

Associate Scientist - Media Formulation

Phyton Biotech, an innovator in the use of plant cell culture technology for the production of ...

Chargeback Coordinator

CITY: Princeton STATE: New Jersey COUNTRY: USA Essential Functions (Responsibilities): Build your ...

BS/MS Research Associate - In vivo Pulmonary/Resp. Diseases research

Our plans for tomorrow are as bold as yours. Schering-Plough has new drugs on the horizon, new ...

Drug Safety Data Entry Specialist - Contract/Temporary Assignment

Genta Incorporated, located in Berkeley Heights, NJ, is an oncology focused pharmaceutical company ...

Senior Medical Writing Scientist (1 of 2)

To learn more about opportunities with the Johnson & Johnson Family of Companies, visit us ...

SSA – Adverse Events

Job Description: Provide support for the review of potential adverse events. To review and assess domestic/international clinical trial and post-marketing surveillance AE reports on marketed products. To determine regulatory reporting requirements based on assessments of seriousness and label...

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