Senior CRA- Trial Start-Up Jobs San Diego
Responsible for clinical activities related to clinical trials and performing or managing daily in-house and outsourced operations associated with these trials. Responsible for regulatory document procedures for study start up activities; including site identification, feasibilities, review and approval, ICF customization and approval, EC and RA submissions, as well as preparation and negotiation of Clinical Site Agreements (CSAs) at a site level.May perform site qualification and initiation visits. Liaises with CROs, Core Labs, and other collaborators to ensure compliance with the Investigational Read more […]