What are the responsibilities and job description for the CLINICAL TRIAL 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.
- Prepare site regulatory documents, eCRFs, paper CRFs, and Clinical Trial Agreements
- Support clinical trial supply and infectious disease sample shipments while adhering to regulatory standards.
- Evaluate suppliers, analyze price proposals, and maintain records of purchased items, costs, and inventories.
- Draft protocol and ICF documents, submit to IRB/EC, and respond to queries.
- Coordinate with data management team to clean and transform raw data for analysis.
- Maintain and update clinical study documents using eTMF.
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