Newark Metro Area, New Jersey
The purpose of the position is to update corporate (CCDS), US and EU labeling (prescribing information and patient information) documents for mature and marketed products to obtain company and/or agency approval, under the supervision of labeling management. Development of labeling for these products is based on study results, coordination of labeling review and approval throughout the company, and preparation of labeling components for submission to regulatory agencies. The position also includes review of local labeling to assure compliance with corporate labeling.
Experience with writing/updating Company Core Labeling (CCDS).
Bachelor's degree in Life Sciences or medically-related field. Minimum of one year experience in the pharmaceutical industry and three or more years in work experience.