Jewellery making

 Data Entry and Verification. Query Generation and Resolutions. Data Base Corrections and Audit Trails. Electronic Delivery of study data sets for interim monitoring and medical review. Delivery and Archiving of Final Study Data Sets.  Reviewing and actioning lab discrepancies. Test and execute validation procedures. Performing the database testing.  To report the issues with the validations and testing status to the client team. To do User Acceptance Testing (UAT) team activities in Clinical Data Management. Handling sCRF and Archiving them.

for (BA/BE studies) providing my professional skills.Key Functions: Developing and writing protocols (outlining the purpose and methodology of a trial).Locating and assessing the suitability of facilities at a study centre.Monitoring the trial throughout its duration, this involved visiting the study centers' on a regular basis.Preparing visit reports from every centre.Managing regulatory authority applications and approvals (that oversee the research and marketing of new and existing drugs).Verifying the data entered into the CRFs is consistent with patient's clinical notes, known as source data/document verification (SDV).Ensuring all unused trial supplies are accounted for.Discussing results with medical statistician, who usually writes technical trial reports.Archiving study documentation and correspondence.Preparing final reports and occasionally manuscripts for publication.Making e CTD submissions.