Ideal candidate is an experienced Clinical Research Associate.
Selected candidates must have 5-10 years (minimum) experience of conducting onsite clinical operations activities - from site selection to site close out, monitoring sites, protocol development, budget and contract negotiation, file audit and maintenance, IRB, ICF, CRF, database review and critical patient results outcome versus study goal.
Experience in device/IVD required. Infectious disease clinical experience is highly recommended.
Must be able to work independently, and travel. No people management skill required.
This is a hands on opportunity. Independent contributor.
Candidates that have no experience with on-site monitoring, inability to travel or strict desire to manage people should not be submitted as they will not be considered.