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!
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