cra i

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThe Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team / local Study Associate Director...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThe Sr CRA must have a minimum 3-5 years' experience as a monitor and can work independently and monitor all stages of a study, in different phases, and should have special therapeutic expertise (oncology). The Sr CRA can take on-board LST tasks and support the LST in coordination or...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Sr CRA I - Sponsor dedicated - Chile Home BasedSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  Our Clinical Development model brings the customer and the patient...