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.