implementation). Collect, capture and track all environmental data for the submission of data into the annual confronting have the ability to compile, analyse and interpret data Must be able to work collaboratively in a team towards
implementation). Collect, capture and track all environmental data for the submission of data into the annual confronting
inspections, errors and corrective action. Analyse quality data and generate reports for management. Ensure that received. Develop and / or update procedurs for capture, investigation and documentation of product complaints
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator
library
Maintain retention sample library
Capturing of QC results on internal system
Filing of
accurate mapping of clinical trial data into a harmonised database, support data acquisition processes, apply notifications, and assist senior staff in improving the data harmonisation platform from a clinical standpoi study
samples etc.) ensuring availability of records for data and root cause analysis. Inform the relevant persons organise data, analyse information and make recommendations. Ability to input data into data capturing software
samples for application work.
Updating and capturing formulatory information in SharePoint Systems
development samples for application work. Updating and capturing formulatory information in SharePoint Systems