- 3+ years of relevant industry or research experience, with pharmaceutical / medical experience is necessary.
- Extremely proficient on OvidSP/Medline and Embase in order to perform clinical and nonclinical literature searches.
- Experience with the most recent Medline and Embase databases.
- Keen understanding of the drug regulatory process such as NDA/IND/Periodic Safety Update annual reporting process.
- Familiar and comfortable with pharmaceutical industry and drug / chemical nomenclature
- Advanced bibliographic expertise in searching and managing information.
Morristown Information Specialist for NDA / Regulatory Submission Job - NJ, 07960