Candidate should be a Male or Female and only qualified as MBBS or MD (candidate qualified as BDS, MDS and any other qualification need not apply)
Ensuring that conduct of the research study adheres to Good Clinical Practice guidelines.
Responsible similar to that of a Principal Investigator (PI) on all study projects.
Liaise with PI in conducting of a study projects.
Obligated to ensure the study is conducted in compliance with applicable laws and regulations and institutional policy governing the conduct of sponsored study.
Where appropriate, there is routine monitoring of the data collected to ensure the safety of subjects present in the study.
Obtaining prospectively and documenting informed consent in accordance with the current IEC-approved informed consent documents
. Reporting promptly to the IEC (and, if applicable, the sponsor and regulatory) any internal or external adverse event that is considered to be unexpected, serious, and possibly or definitely related to the study
Maintaining adequate and accurate research subject records to reflect adherence to protocol specific requirements
Documenting the delegation of study responsibilities to qualified and adequately trained staff. Supervising study performance and overseeing the performance of study staff at the study sites.