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 requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator 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 requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
up to standard