trial to ensure protocol and GCP compliance
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment Medical Importance as per protocol requirements. Quality control of patient files and data entries (i.e., eCRF's visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment Medical Importance as per protocol requirements. Quality control of patient files and data entries (i.e., eCRF's visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
rt budget development with senior management, control and monitor expenditures of the clinic, adhering clinic; and compliant and effective safety, quality control, and record keeping of medicine at hand
Support budget development with senior management, control and monitor expenditures of the clinic, adhering clinic; and compliant and effective safety, quality control, and record keeping of medicine at hand Attend analysis and utilization Good understanding of quality improvement systems, monitoring and evaluation
Support budget development with senior management, control and monitor expenditures of the clinic, adhering clinic; and compliant and effective safety, quality control, and record keeping of medicine at hand Attend analysis and utilization Good understanding of quality improvement systems, monitoring and evaluation
up to standard