Clinical Research Principal Investigator (Psychiatrist, MD)
Confidential
Posted: February 9, 2026
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Quick Summary
Elevate Clinical Research is seeking a full-time Psychiatrist (MD) to serve as a Principal Investigator (PI) for industry-sponsored and investigator-initiated clinical trials. The ideal candidate will have experience in psychiatric research, maintain an active and unrestricted medical license, and be willing to travel between two local research locations.
Required Skills
Job Description
Elevate Clinical Research is seeking a full-time Psychiatrist (MD) to serve as a Principal Investigator (PI) for industry-sponsored and investigator-initiated clinical trials. The ideal candidate will have experience in psychiatric research, maintain an active and unrestricted medical license, and be willing to travel between two local research locations.
This role offers the opportunity to lead high-quality psychiatric clinical trials within a growing research network supported by strong operational infrastructure.
Practice Locations
The PI will rotate between the following research sites:
5132 Atascocita Rd., Humble, TX 77346
1045 Gemini St., Suite 200A, Houston, TX 77058
Travel between sites is required as part of routine study oversight and subject care.
Key Responsibilities
Serve as Principal Investigator on psychiatric clinical trials, ensuring compliance with:
FDA regulations
ICH-GCP guidelines
Sponsor protocols and IRB requirements
Conduct and supervise:
Psychiatric evaluations and diagnostic assessments
Study visits and dosing oversight (as applicable)
Act as Lead Rater for psychiatric rating scales and ensure rater quality across studies, including:
Administration of clinician-rated efficacy scales (e.g., MADRS, CGI, YMRS, PANSS, C-SSRS, etc.)
Oversight, calibration, and consistency of ratings across visits
Participation in sponsor-required rater training, certification, and re-calibration
Ensure subject safety, data integrity, and protocol adherence
Oversee and collaborate with:
Sub-Investigators
NP/PA providers
Research coordinators and support staff
Participate in:
Sponsor and CRO meetings
Site initiation visits (SIVs)
Monitoring visits, audits, and inspections
Review and sign off on:
Source documentation
eCRFs
Adverse event and serious adverse event reporting
Support the strategic expansion of the psychiatric research portfolio, including novel and emerging therapeutics
Qualifications
MD or DO with board eligibility or board certification in Psychiatry
Active, unrestricted medical license (clean license required)
Prior experience as a Principal Investigator or Sub-Investigator in clinical research preferred
Demonstrated experience with psychiatric rating scales and structured interviews
Ability to work effectively in a regulated research environment
Willingness to travel between both clinical locations
Strong leadership, documentation, and communication skills
Preferred Experience
Industry-sponsored trials in:
Major depressive disorder
Treatment-resistant depression
Anxiety and related mood disorders
Experience serving as Lead Rater or primary rater
Familiarity with electronic source, EDC, and CTMS systems
Experience working with NPs/PAs in collaborative psychiatric settings
Employment Details
Full-time position
Competitive compensation (commensurate with experience)
Full research and administrative support provided
Opportunity for growth within a rapidly expanding clinical research network