Design IRT systems for clinical trials
Take the client protocol
Translate to user requirement spec
Resp for clinical study from study award to go live then goes to the client services PM
Specification / Co-ord of activities. Validation / resp for UAT / go live activities /. Study finances and budgets (not the budget holder but must adhere to budget proposal and adapt budget accordingly)
Co-ord efforts for all other team who do things like user guides, investigator meeting slides etc .
PM – more BA than a tech person who translates to a document that the client can understand but technical enough for the tech people to build
System design – clinical systems such as CTMS / EDC / DMS
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com