Protouch Staffing
Clinical Research GI - Houston , TX
Job type: Part-time
Shift: Days
Job Description:
We are seeking a board-certified to serve as a Clinical Research GI. You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.
Key Responsibilities:
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials. Conduct medical screenings, dermatological assessments, and physical examinations for study participants. Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements. Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation. Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems. Qualifications:
M.D. or D.O. with an active, unrestricted TX medical license. Board certification in required. Valid DEA license and BLS/ACLS certification. Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates). Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS). Benefits:
All standard benefits are provided.
Job type: Part-time
Shift: Days
Job Description:
We are seeking a board-certified to serve as a Clinical Research GI. You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.
Key Responsibilities:
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials. Conduct medical screenings, dermatological assessments, and physical examinations for study participants. Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements. Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation. Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems. Qualifications:
M.D. or D.O. with an active, unrestricted TX medical license. Board certification in required. Valid DEA license and BLS/ACLS certification. Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates). Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS). Benefits:
All standard benefits are provided.