Job Description

Job Responsibilities

• Serve as the Principal Investigator for assigned clinical trials, ensuring regulatory compliance and high standards of clinical oversight.
• Supervise study conduct, participant safety, and data integrity in accordance with FDA, GCP, and IRB guidelines.
• Collaborate with the clinical and operational team to ensure timely and accurate trial execution.
• Participate in protocol training and site initiation as required.
• Provide leadership and oversight of clinical research staff, ensuring patient safety and adherence to study protocols and regulatory requirements.
• Attend Investigator Meetings (IMs) and participate in continuing education to stay current with medical and clinical trial advancements.
• This position will be onsite
• Contract starting at 8 hours per week (one day) once the trial is up and running 2 days a week (so ideally two days available, starting with one) These days can be flexible
• Start ASAP

Job Requirements:

• Must be Hybrid in Dallas, TX
• PI experience would be beneficial but not required
• No travel commitments other than onsite, days onsite can be flexible to suit the candidates availability

License/Certification

• Board certified Psychiatrist
• License to practice in TX

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