Clinical Investigator
7 days 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 - ₹900,000.00 per year
**Benefits**:
- Food provided
Schedule:
- Night shift
- Rotational shift
Supplemental Pay:
- Performance bonus
Work Location: In person
Application Deadline: 10/06/2025
Expected Start Date: 29/05/2025
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Bengaluru, India MS CLINICAL RESEARCH Full timeJob SummaryThe Clinical Operations Manager will lead and oversee end-to-end clinical study execution across Skin, Hair, and Oral domains. This role is responsible for managing study operations, ensuring compliance with protocols, SOPs, and regulatory guidelines, and coordinating with internal teams, investigators, and sponsors. The candidate will ensure...
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Bengaluru, India MS CLINICAL RESEARCH Full timeJob Summary The Clinical Operations Manager will lead and oversee end-to-end clinical study execution across Skin, Hair, and Oral domains. This role is responsible for managing study operations, ensuring compliance with protocols, SOPs, and regulatory guidelines, and coordinating with internal teams, investigators, and sponsors. The candidate will ensure...
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Bengaluru, India MS CLINICAL RESEARCH Full timeJob Summary The Clinical Operations Manager will lead and oversee end-to-end clinical study execution across Skin, Hair, and Oral domains. This role is responsible for managing study operations, ensuring compliance with protocols, SOPs, and regulatory guidelines, and coordinating with internal teams, investigators, and sponsors. The candidate will ensure...
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