Hi, i completed my Master's in biotechnology. Then i did advanced post graduate diploma in Clinical trials & QA management and also did 6 months diploma in Clinical data management.
Recently I did 2 months Internship in CDM (at company).
Experiences:
CRF designing (Openclinica drive, Medidata rave, & adobe live cycle)
Data entry in clinical data management
Data validation, C-disk etc.,
Source data verification & monitoring activities
Skills:
ICH gcp guidelines, Shedule Y, EMEA, US FDA
Microsoft office - Word, Exel, Power point
Adobe live cycle 8.3
Openclinica drive
Medidata Rave