Job Description & How to Apply Below
About the job
Pay: $18–$36 per hour (₹1,500–₹3,000 per hour)
Engagement:
Part-time | Contract (3–4 hours/week)
Location:
Delhi
About VI Signal Inc.
VI Signal Inc. is developing Face Echo, an AI-powered facial scan and questionnaire-based application designed to identify visual patterns associated with wellness and health-related indicators. The platform uses structured front-face, multi-angle, and guided video scans combined with symptom questionnaires to generate pattern-based insights.
The system is non-diagnostic and intended to support research, early signal detection, and follow-up recommendations such as consultation or laboratory evaluation. The current study aims to evaluate the accuracy, consistency, and safety of these pattern-based observations while ensuring ethical deployment and appropriate clinical oversight.
The study will be conducted as a clinical accuracy and research validation effort focusing on scientific rigor, participant safety, and responsible use of AI-based pattern detection.
This study will be conducted in India, with a preference for Maharashtra, while supporting a predominantly remote participation model with some guided participation where applicable.
Role Summary
We are seeking a Principal Investigator (PI) to provide scientific and ethical oversight for a clinical accuracy study evaluating an AI-based facial scan and questionnaire system.
The study evaluates pattern-based detection signals across multiple wellness and medical-related indicators. The system is non-diagnostic and intended for research and validation purposes.
The PI will be responsible for ensuring ethical compliance, participant safety, scientific validity, and appropriate study governance throughout the study lifecycle, including oversight of study processes, participant safety frameworks, and data interpretation standards.
Key Responsibilities
1. Study Oversight
Review and approve study protocol
Validate study objectives and endpoints
Ensure alignment with non-diagnostic positioning
Provide guidance on study design considerations
2. Ethics Oversight
Review and approve:
User Consent Form
Participant Information Sheet
Risk Disclosure Statement
Ensure voluntary participation framework
Confirm appropriate participant communication
Oversee participant safety considerations across study settings
3. Clinical Reasonability Review
Validate inclusion of study conditions
Confirm plausibility of visual signal detection
Ensure messaging avoids diagnostic interpretation
Advise on follow-up recommendation positioning
4. Reviewer Panel Oversight
Approve reviewer structure (two reviewers and tie-breaker)
Provide guidance on disagreement resolution
Oversee consistency of clinical review approach
Conduct sample-based review of outputs
5. Study Monitoring
Participate in scheduled weekly checkpoints
Review sample outputs for safety and consistency
Ensure ethical compliance throughout the study
Provide guidance on required adjustments across remote and guided participation formats
6. Documentation & Scientific Contribution
Protocol approval
Ethics oversight confirmation
Study completion acknowledgment (if applicable)
Contribution to study interpretation, reporting, and scientific outputs (including publication)
Scope of Involvement
The PI will provide oversight and guidance across:
study ethics
clinical plausibility
participant safety
reviewer alignment
messaging and communication
study governance
interpretation of study findings
Expected Time Commitment
Approximately 3–4 hours per week during the active study period, including:
weekly oversight meetings
sample-based review
ethics and safety monitoring
guidance to reviewer panel
Additional time may be required for initial protocol review and final study oversight.
Required Qualifications
MBBS / MD / equivalent medical degree
Licensed physician (India)
Experience in clinical practice or research
Understanding of clinical evaluation studies
Recent ethics training (e.g., ICMR/National Ethics Guidelines or equivalent)
Preferred Qualifications
Experience in digital health or AI-based tools
Prior research oversight experience
Ethics committee exposure
Telehealth familiarity
General Physician / Internal Medicine preferred
Reporting Structure
1) PI Collaborates With:
Product team
Research team
Reviewer doctors
2) PI Oversees:
Study ethics
Scientific integrity
3) Deliverables
Protocol approval
Ethics review confirmation
Reviewer structure approval
Weekly oversight feedback
Final oversight note
Contribution to study reporting and publication
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