Principal Investigator (Glocare Labs – CRO)

Role Description

We are currently hiring for a Principal Investigator role with a Clinical Research Organization (CRO) setup.

The role requires a qualified medical doctor with hands-on experience in Bioavailability / Bioequivalence (BA/BE) studies, who can take full responsibility for study conduct, subject safety, and regulatory compliance.

Qualifications

• Act as Principal Investigator for BA/BE studies
• Provide medical oversight during screening, dosing, and study execution
• Ensure compliance with ICH-GCP, DCGI / CDSCO guidelines, and regulatory requirements
• Review and approve - Study protocols, Informed consent documents, Clinical study reports
• Oversee subject safety and adverse event management
• Coordinate with Ethics Committees and regulatory bodies
• Ensure audit readiness and inspection compliance
• Supervise clinical and study teams to ensure data integrity and protocol adherence

Candidate Profile:

MBBS (mandatory) with experience in BA/BE studies in a CRO or

MD in Pharmacology with relevant clinical research / BA/BE exposure

Experience Requirement:

• Hands-on experience in BA/BE study execution
• Experience working in a Clinical Research Organization (CRO)
• Prior experience as Principal Investigator or Co-Investigator preferred

Strong understanding of:

• ICH-GCP
• Regulatory compliance (DCGI / CDSCO)
• Clinical study processes

What We Are Looking For:

• Strong medical and regulatory accountability
• Ability to independently lead and oversee studies
• Experience handling audits / inspections
• High level of professional integrity and documentation discipline