• PRA Health Sciences
  • Williamstown , NJ
  • Pharmaceutical/Biotechnology
  • Full-Time
  • 398 W Malaga Rd


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Responsibilities

You will be responsible for supporting clinical trials including, but not limited to, clinical documentation, coordinating team meetings, taking meeting minutes, ordering supplies for study sites, and QC of data for clinical studies. You will create spreadsheets for reporting, generate reports and log documents. You will be supporting a variety of groups within the company so flexibility is key!

Qualifications

Qualifications:

  • 1+ years of previous experience supporting clinical trials
  • TMF experience is preferred
  • Experience with SharePoint and Excel is preferred
  • Exhibits proficiency in managing multiple projects and deliverables with competing priorities
  • Bachelor s Degree preferred in scientific/medical discipline or equivalent experience
  • Read-write and speak fluent English

  • Associated topics: clinical, clinical development, clinical informatics, clinical trial, coordinator, lab, laboratory, research, research coordinator

    * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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