Job Description

We are seeking a skilled and experienced Psychiatrist to join our team as a Principal Investigator at a clinical research site in Dallas, TX . The primary focus will be on conducting

psychological assessments but not limited when needed for oversight of all clinical trial studies according to study protocols, company processes and GCP.

Job Responsibilities

• Your main focus will be overseeing clinical evaluations and assessment
• HAM-A, SCID-5, CGI-I and CGI-S, ATRQ and MADR
• Ensure the safety and well-being of study participants throughout the clinical trial
• You will supervise site personnel to ensure adherence to safe trial procedures and best practices
• Assess and report on screening failures, safety outcomes, and participant retention metrics
• Collaborate regularly with IRBs and study sponsors to ensure compliance and alignment
• Adhere to study protocols, SOPs, GCP guidelines, and state regulations in all medical duties
• Analyze clinical trial data to identify trends and insights
• Compile comprehensive reports with findings and recommendations for process enhancements
• Stay informed on the latest SOP updates and documentation standards
• This is a part-time role with flexible hours, ranging from 5-20 hours per week. The schedule will vary based on the clinical trial's requirements, providing adaptability and the chance to contribute to a dynamic and engaging research project

Job Requirements:

• At least 2 years of experience as a Principal Investigator or Sub-Investigator
• Strong analytical abilities to collect, assess, and interpret complex data.
• Exceptional written and verbal communication skills for report writing and presenting findings.
• Proven ability to lead a team and manage priorities in a fast-paced setting.
• Keen attention to detail and a strong commitment to maintaining confidentiality with sensitive information.

License/Certification:

• DEA License (Required)
• Texas MD License (Required)

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