Experience

TRIO - Translational Research in Oncology

• Canada
• Research Services
• 100 - 200 Employee

• Clinical Data Specialist

  • May 2021 - Present

  • Reviewing clinical data relating to patients /sites collected through Case Report Form (eCRF) in order to ensure accuracy of the data in compliance with the protocol trial written instructions. • Generating queries in the clinical database (iMedidata and Elluminate) where inconsistencies or missing data has been reported • Follow up on the queries by reviewing answers until they are appropriately resolved by the sites and close them once adequate resolution of the issues found. • Tracking any protocol deviations and non-protocol deviations identified during the data validation process in the Clinical Trial Management system (CTMS) and informing the concerned CRA/SM. • Performing quality checks of protocol deviations reported in CTMS • Contacting CRAs and Study Managers as needed to resolve site specific issues. • Contacting CRAs, SMs and Monitoring resources coordinator’s (MRC) as required in case of specific issues and provide support for CRF completion questions • Contributing to the development or in reviewing trial documents associated with data validation activities (e.g. data validation written instructions, validation tools specifications, annotated validation tools, trial written instructions, etc.) • Participating in the global PM call to communicate information or trends identified during data review • Participating in the review of other study documents (e.g. guidelines, specifications, newsletters, manuals and reports) associated with data validation activities • Participating in aggregate review of data listings during IDMC and Interim Analysis (IA). Performing deep crosschecks between datalistings using microsoft excel tools (conditional formatting, filters, etc) • Participating in presenting training topics and in on boarding activities for new data validation specialists • Participating in global quality checks of protocol deviations reported under the CTMS • Communicating with Safety and Medical Monitoring team regarding SAEs.



Dynacare

• Hospitals and Health Care
• 700 & Above Employee

• Laboratory Assistant-Specimen processing

  • Apr 2021 - May 2021

  -Enter all patients data and test information for requisitions accurately - Manage COVID-19 samples - Process add-on test requests and subsequent specimen selection. - Process all specimens including receiving, sorting, labeling, separation, and placing in appropriate area. - Follow all guidelines for the handling of infectious material. - Prepare specimens and documentation for reference testing. - Ensure type of sample is correct for specified test and sent to correct reference laboratory.



Department of Human Genetics, Guru Nanak Dev University

• Amritsar, Punjab (INDIA)

• Doctor of philosophy

  • Aug 2014 - Dec 2019

  Served as "Ph.D scholar" under University with Potential for Excellence (UPE) grant provided to Guru Nanak Dev University, Amritsar by the University Grant Commision (UGC), New Delhi. The work was conducted under the guidance of Dr. Badaruddoza 1. Sample collection from hospitals and clinics 2.Sample processing in lab 3. Data collection and entry on Microsoft excel sheet 4. Statistical Analysis 5. Interpretation of Results Served as "Ph.D scholar" under University with Potential for Excellence (UPE) grant provided to Guru Nanak Dev University, Amritsar by the University Grant Commision (UGC), New Delhi. The work was conducted under the guidance of Dr. Badaruddoza 1. Sample collection from hospitals and clinics 2.Sample processing in lab 3. Data collection and entry on Microsoft excel sheet 4. Statistical Analysis 5. Interpretation of Results



National Agri-Food Biotechnology Institute

• Mohali, Punjab (INDIA)

• Project Assistant

  • Nov 2013 - May 2014

  The project involved the metabolite profiling and the data analysis. The practical expertise over handing LC-MS, GC-MS and ICP-MS was acquired. The project involved the metabolite profiling and the data analysis. The practical expertise over handing LC-MS, GC-MS and ICP-MS was acquired.