Clinical Research Coordinator
International Medical Center
مجموع سنوات الخبرة :14 years, 10 أشهر
Handles all works related to Clinical trial initiation, conduct, audit and data management.
Responsible for providing statistical support for the biomedical research works done at the institution.
Provides workshop on clinical triala and biostatistics.
Provides the support required for setting up disease registeries and database creation.
Maintains and updates the Research center website at institution.
A member of IRB commitee and overviews the Ethical aspects of biomedical and clinical trials.
Provides necessary guidances in applying the research proposals for IRB review at the institution.
Handson experience on SPSS and provides the data analysis support for all research related works.
Research paper articulation and related works
Was responsible for data validation of Clinical data and programming of edit checks
Was able to create, update various tracker and reports required by PDM, CROs and sponsors
Was able to follow the GCP guidelines and do regular tutorials and workshops on GCP.