2 data entry intern jobs found

SOFTWARE DEVELOPERS: Princeton, NJ & various unanticipated locations throughout US: Dsgn, dvlp & mntn apps, RESTful APIs, Web Srvcs & Microsvcs. Utlz Entty Frmwrk Core, LINQ to strmln data quryg & trnsfrmtns. Dvlp dynmc & rspnsv web apps & usr frndly intrfcs. Intgrt Dpndncy Injctn. Work w/micro frntend archtctr to handle cmplxty of lrg apps. Wrt SQL quers, strd prcdrs & trggrs. Cndct API tstg & versnng. Skills reqd: C#, .Net, Net Core, Angular, HTML5, CSS3, Bootstrap, API, PostgreSQL, & Postman. Bachelors in Sci, Tech, or Engg (any) +2 yrs exp in job offrd or rltd occup reqd. Salary: $103,210/yr. Email CV: HR, Adya Technologies, Inc DBA Fugen Solutions, hr@fugeninc.com recblid sxxd8pk4youarw1d1b0z4ngp7yupif

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...