Overview
We have an urgent requirement for full - time Principal investigator in Clinical Research with a candidate having experience 0-2 years. Preferably Male.
To ensure that all necessary study related documents are generated and are compliant with the protocol.
To enroll healthy volunteers as per the inclusion / exclusion requirements of the protocol. To ensure subjects fitness prior to dosing and then to supervise dosing of subjects. To supervise the activities like check-in or blood sampling and sample separation. To ensure that the diet specifications as per the protocol are met. To maximize the trial subjects protection by effective management of adverse events and ensure that subjects well being and safety is the foremost priority. Timely intimation to the sponsor and Ethics committee of any serious adverse event in a study.
All the best! - 
