#x 2022; Serve as the study physician for assigned trials; ensure participant safety and ethical conduct. - Review and confirm participant eligibility; oversee screening outcomes, A - Es/ SA - Es, and retention trends. - Perform/oversee study-specific medical assessments (histories/physicals, concomitant meds, endpoint review). - Provide medical oversight to site staff (Sub-Investigators, CR - Cs, RNs, lab staff); be available for consults and safety questions. - Collaborate with IR - Bs, sponsors, and CROs; join SI - Vs, monitoring visits, and close-out activities as needed. - Ensure compliance with protocols, site SOPs, ICH-GCP, FDA/21 CFR, and Arizona or Texas state requirements (as applicable). - Review clinical data (labs, EC - Gs, vitals) and support timely safety reporting and documentation. - Contribute to high-quality source documentation, query resolution, and continuous improvement of site processes. Minimum Qualifications: - MD or DO (Family or Internal Medicine). - Active, unrestricted Arizona Medical Board license, as applicable. - Experience in clinical research and comfort reviewing structured clinical data. - Strong documentation, communication, and confidentiality practices (HIPAA/ PHI). Preferred Qualifications: - Prior experience as a PI or Sub-Investigator (training provided for the right candidate). - Familiarity with ICH-GCP and FDA regulations (21 CFR Parts 50, 54, 56, 312, 812). - Board certification in Family or Internal Medicine. - DEA registration – Schedule I or II license, or are willing to obtain this license. 10233905