What are the responsibilities and job description for the DRUG SAFETY ASSOCIATE (multiple openings) position at Zenith LifeScience?
Department: Quality & Regulatory Compliance (Clinical Operations)
Zenith LifeScience LLC has multiple openings in South Plainfield, NJ and other unanticipated locations nationwide for positions requiring at least one year of relevant experience, to perform duties the following duties:
Responsibilities:
- Coordinate and document internal regulatory processes for pharmaceutical clinical studies.
- Receive, evaluate and report Serious Adverse Event (SAE) reports from clinical trials.
- Submit SAE reports to regulatory agencies.
- Perform quality review of Adverse Event data entry, MedDRA, WHO-Dictionary coding, Narratives and labeling of cases.
- Assist validation department by authoring and executing scripts for safety database upgrades.
Educational and/or experience requirements:
- Master’s degree or equivalent in Science, Engineering, Pharmacy or related field with at least one (1) year of relevant experience.
- Travel/relocation required to various unanticipated client work locations nationwide for long or short durations and unknown frequency.
Job Type: Full-Time
Offered salary: $111,925.00 / Year
Mail two copies of resume and proof of work eligibility to: 51 Cragwood Rd., Suite 306, South Plainfield, NJ 07080.
– Posted on 07/16/2025
Salary : $111,925