Psychiatrist Clinical Research - Houston , TX

ProTouch Staffing

Houston, TXPart-time and Contractor

100–250 an hour

Behavioral Health Market Context

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Job Description

nvestigator (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).
• Strong interpersonal and communication

Benefits:
• All standard benefits are provided.

For more information, please reach out to Dheeraj Mohan: at (469) 430-0547 or by Email: at [email protected].

Qualifications

  • M.D. or D.O. with an active, unrestricted TX medical license
  • Board certification in required
  • Valid DEA license and BLS/ACLS certification
  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS)
  • Strong interpersonal and communication

Benefits

  • All standard benefits are provided

Responsibilities

  • 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
  • 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


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