the clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate well with requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings systematic in approach to tasks, with strict compliance to protocols Exceptional organizational and administrative
the clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate well with requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings systematic in approach to tasks, with strict compliance to protocols Exceptional organizational and administrative