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 Overseeing Investigational product accountability Shall be responsible for all study-related medical decisions Shall be responsible for ensuring the accuracy completeness legibility and timeliness of all study data that are reported to the Sponsor Job Type Full-time Pay 720 000 00 - 900 000 00 per year Perks Food provided Work Location In person Application Deadline 31 07 2025 Expected Start Date 23 07 2025

📌 Clinical Investigator (Karnataka)
🏢 Notrox Research Private
📍 Karnataka