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DRUG SAFETY ASSOCIATE (multiple openings)

Zenith LifeScience
South Plainfield, NJ

Apply Now

Job Details

Full-time
$111,925 a year

Qualifications

Adverse event reporting
Clinical incident reports
Mid-level
Adverse drug reaction monitoring
Clinical data report preparation
Scripting
Document review
Pharmacy
Clinical trial patient safety management
Regulatory submissions
Database migration or upgrading
Clinical quality assurance standards
1 year
Master's degree in engineering
Legal compliance
Clinical data audit

Full Job Description

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

Apply Now

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various openings jobs

DRUG SAFETY ASSOCIATE (multiple openings)

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