Principal Investigator

Key Responsibilities

• Serve as Principal Investigator for clinical trials conducted in Texas
• Provide medical oversight and ensure participant safety throughout the study lifecycle.
• Review study protocols, informed consent documents, and case report forms.
• Perform physical exams, review inclusion / exclusion criteria, and assess adverse events.
• Ensure compliance with regulatory, Good Clinical Practice (ICH GCP), and sponsor protocol.
• Collaborate with site staff to maintain accurate documentation and data integrity.
• Participate in sponsor / CRO visits, audits, and inspections as needed.
• Represent client in interactions with sponsors, CROs, and regulatory authorities.

Qualifications