Psychiatrist Clinical Research - Houston , TX
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].
• 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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