Job Description

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

• MD or DO with an active medical license in Texas.
• Board certification in Internal Medicine, Family Medicine, Infectious Disease, or specialty
• Prior experience as a Principal Investigator or Sub-Investigator in clinical trials
• Strong communication, leadership, and organizational skills.
• Commitment to patient safety and ethical conduct of clinical trials.

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