• Conduct on-site clinical monitoring which includes: document review, ensuring accurate data recording, verifying patient data, adherence to the protocol of a clinical trial in accordance with GCP/ICH guidelines• Perform on-site visits, including site qualification, initiation, monitoring and close out visits.• Maintaining the study related logs – screening, enrolment, drug administration, temperature and all the other logs as per SOPs.• Managing the accountability of the Clinical… Show more • Conduct on-site clinical monitoring which includes: document review, ensuring accurate data recording, verifying patient data, adherence to the protocol of a clinical trial in accordance with GCP/ICH guidelines• Perform on-site visits, including site qualification, initiation, monitoring and close out visits.• Maintaining the study related logs – screening, enrolment, drug administration, temperature and all the other logs as per SOPs.• Managing the accountability of the Clinical Trial Material and Investigational Medicinal Product.• Review monitoring findings or any serious deficiencies discovered during the monitoring visit and discuss with the Senior Manager. Show less