
Clinical Investigator
1 week ago
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.
- 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
- 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.
Pay: ₹720,000.00 - ₹780,000.00 per year
**Benefits**:
- Food provided
Schedule:
- Rotational shift
Supplemental Pay:
- Performance bonus
**Education**:
- Bachelor's (required)
Work Location: In person
Application Deadline: 15/03/2025
Expected Start Date: 07/03/2025
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