Clinical Research Nurse I - Lombardi Comprehensive Cancer Center
... staff, physicians, IRB, review committees, clinical research finance team, and auditors.Act as a liaison with sponsors during study start-up activities and participate ...
... staff, physicians, IRB, review committees, clinical research finance team, and auditors.Act as a liaison with sponsors during study start-up activities and participate ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... with the relevant Global PDT Clinical Science Study Management (CSSM) indication specific leads on EMEA regional clinical trial assignments. Identify, establish and ...
... ambition to support future state clinical trial executionLead and support all study start up activities leading, site ... and advancement of the clinical organization.Bachelor’s degree in science or related area of study Preferred• Advanced degree (E.g., ...
... coordination of assigned clinical trials throughout the trial lifecycle.Collaborate with investigators and more senior study team members by participating in ... staff) along with clinical trial sponsors, auditors, and study monitors. S he performs all ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... focus areas include developing a study design that answers the relevant questions of the clinical trial and optimally uses existing ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...