Zenith LifeScience LLC
Plainfield, NJ
Pharmaceutical Professionals
Zenith Lifescience LLC has multipleopenings in So. Plainfield, NJ & otherunantcptd locns nationwide for positionsrequiring min
1 yr of relevant exp, to
perform duties the following duties:
Clinical Trial Associate
Coord & documt internal regulatoryprocesses for pharmal clinical studies.
Prepare site regulatory documts,eCRFs, paper CRFs, & Clinical Trial Agreements. Support clinical trialsupply & infectious disease sampleshipments while adhering toregulatory standards. Evaluate suppliers, analyze price proposals,& maint records of purchased items,costs, & inventories. Draft protocol& ICF documts, submit to IRB/EC,& respond to queries. Coord w/datamgmt team to clean & transform rawdata for analysis. Maint & updateclinical study documents using eTMF.
Drug Safety Associate
Coord & documt internal regulatoryprocesses for pharma clinical studies.Receive, evaluate & report SeriousAdverse Event (SAE) reports...