Clinical DB Designer, IQVIA

Design and update eCRF, Create and update Edit Specification Document, Generate specifications for EDC build components, Complete Study Authorization Form and Trial Capacity Request Form, Attend review meetings, Design database for LLRR data, Communicate project risks, Ensure completion of training, Conduct pre-design and edit specification meetings

Interpret study protocol, Design and update eCRF, Create Edit Specification Document, Generate specifications for EDC build components, Complete Study Authorization Form, Attend review meetings, Design database for LLRR data, Communicate project risks, Ensure training completion

Bachelor's Degree (B.Tech, BCA, etc.), 0-2 years experience