Hard Skills
AdvancedGood Clinical Practice (GCP) ComplianceApplying international ethical and scientific quality standards for clinical trials involving human subjects.
AdvancedClinical Trial MonitoringOverseeing the progress of a clinical trial and ensuring it is conducted and recorded in accordance with the protocol.
IntermediateBiological Sample ManagementManaging the collection, processing, storage, and shipping of biological specimens according to scientific protocols.
AdvancedPharmacovigilance and Safety ReportingIdentifying, documenting, and reporting Adverse Events (AEs) and Serious Adverse Events (SAEs) to regulatory bodies.
IntermediateElectronic Data Capture (EDC) ProficiencyUsing specialized software systems to enter, manage, and verify clinical trial data.
IntermediateRegulatory Document MaintenanceEnsuring all essential trial documents are present and updated in the Trial Master File (TMF).