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The CRA will take charge of keeping investigative reports and providing project communications between the various sites.
The CPM position will perform a wide variety of activities to support the start-up and completion of clinical research studies.
The Sr Manager Regulatory Affairs will assist in determining the regulatory strategies of all branded products in clinical development.
The Senior Director Regulatory Affairs will determine the regulatory strategies of all products in clinical development
Help develop a AI ML translation solution for the labeling and publishing groups of a global pharma client