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 patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings, SIV, and any other key meetings 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 patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings, SIV, and any other key meetings visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
related equipment
and record keeping of medicine at hand
control, and record keeping of medicine at hand Attend to all staffing requirements & administration
control, and record keeping of medicine at hand Attend to all staffing requirements & administration