Rakesh H.

- working for medical device industry, document writing , quality check, data entry, data management - Web Research for Investigator Personnel and site Information with 100 % quality meeting the client expectation and validate it to the database using Java Application -Primarily research based on Trial posting URLs (, etc) or journals or from Conference information. -Well versed in MS Office -Appreciation by client based on web research - Quality check for documentation prepared by team members -Coordinate and assist the study coordinators and investigator in managing the clinical operations related to conduct of the trial (i.e. study document preparation, recruitment, informed consent procedure, visit coordination, sampling, visit scheduling, etc). -Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), and electronic CRFs -Responsible for CTRI registration and Import Export process