Psychiatrist (MD/DO) – Clinical Research
Lighthouse Psychiatry Brain Health Center
·Yesterday
- Location
- Gilbert, Arizona, US
- Type
- Contract
- Department
- Healthcare
- Education
- Master
- Source
- BetterTeam
Description
Focus: Clinical Research | Psychiatry | Clinical Trials
- Serve as a Principal Investigator (PI), Sub-Investigator, or physician investigator depending on qualifications and study requirements.
- Provide physician oversight for psychiatric clinical trials.
- Evaluate prospective research participants and determine medical and psychiatric eligibility.
- Review and confirm study inclusion and exclusion criteria.
- Conduct protocol-required psychiatric evaluations and research visits.
- Participate in and oversee the informed consent process.
- Perform or oversee protocol-required psychiatric assessments and rating scales.
- Review medical histories, concomitant medications, laboratory results, ECGs, and other study-related clinical data.
- Evaluate, document, and follow adverse events (AEs) and serious adverse events (SAEs).
- Assess the clinical significance and study-treatment relationship of adverse events when required.
- Ensure appropriate participant safety monitoring throughout study participation.
- Review and sign source documentation, study records, and investigator documentation as required.
- Maintain appropriate investigator oversight and ensure adherence to study protocols.
- Identify, document, and appropriately address protocol deviations.
- Collaborate with clinical research coordinators and other research personnel.
- Work with pharmaceutical and biotechnology sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), monitors, central laboratories, pharmacies, and other study vendors.
- Participate in site qualification, site initiation, monitoring, closeout, and sponsor visits.
- Attend investigator meetings and study-specific training.
- Review and respond to clinical and research data queries.
- Support regulatory documentation and investigator responsibilities.
- Maintain compliance with ICH-GCP, FDA regulations, IRB requirements, HIPAA, study protocols, and applicable federal and state regulations.
- Maintain required research training and study-specific certifications.
- Participate in quality assurance and research compliance activities.
- Contribute to the development and expansion of Lighthouse Psychiatry's clinical research program.
- Overall medical and scientific oversight of assigned clinical trials.
- Ensuring studies are conducted according to the approved protocol, investigator agreement, GCP, and applicable regulatory requirements.
- Maintaining appropriate delegation and oversight of research personnel.
- Reviewing participant eligibility and safety.
- Reviewing safety reports and clinically significant findings.
- Ensuring appropriate documentation of protocol deviations and safety events.
- Providing oversight of investigational product-related clinical decisions.
- Participating in sponsor and CRO communications.
- Supporting regulatory inspections and research audits.
- Reviewing study performance, enrollment, retention, and data quality
- Maintaining appropriate investigator availability and supervision.
- Principal Investigator development and mentorship.
- Industry-sponsored Phase II–IV psychiatric clinical trials.
- Investigator-initiated studies.
- Treatment-resistant depression research.
- Psychopharmacology research.
- Neuromodulation research.
- TMS and brain-stimulation research.
- Ketamine and emerging therapeutic research.
- Novel psychiatric medications and investigational therapeutics.
- Biomarker and neuroscience research.
- Research protocol development.
- Scientific presentations, abstracts, posters, and publications.
- Collaboration with pharmaceutical and biotechnology companies.
- Collaboration with CROs, academic institutions, and research organizations.
- Development of new psychiatric clinical trial programs.
- MD or DO degree from an accredited medical school.
- Completion of an accredited Psychiatry residency.
- Board-Certified in Psychiatry.
- Active, unrestricted Arizona medical license.
- No state or federal sanctions on medical license.
- Active DEA registration or eligibility, when required by study responsibilities.
- Strong psychiatric diagnostic and clinical assessment skills.
- Ability to evaluate research participants and make independent medical safety decisions.
- Strong documentation, organizational, and communication skills.
- Commitment to participant safety, research integrity, and regulatory compliance.
- Previous experience as a Principal Investigator, Sub-Investigator, or clinical research investigator.
- Experience conducting psychiatric clinical trials.
- Good Clinical Practice (GCP) certification or willingness to complete required training.
- Familiarity with FDA-regulated clinical research.
- Familiarity with IRB processes and human-subject research requirements.
- Experience with pharmaceutical or biotechnology-sponsored clinical trials.
- Experience working with CROs and clinical research monitors.
- Experience with psychiatric rating scales and structured research assessments.
- Research publications, presentations, or previous academic research experience.
- Interest in psychopharmacology, neuroscience, treatment-resistant depression, neuromodulation, or emerging psychiatric therapeutics.
- Dedicated clinical research-focused physician role.
- Opportunity to participate in innovative psychiatric clinical trials.
- Clinical research coordinator and administrative research support
- Opportunities to work with pharmaceutical, biotechnology, and CRO partners.
- Development pathway toward Principal Investigator (PI) responsibilities.
- Exposure to emerging psychiatric medications and therapeutic technologies.
- Opportunities for scientific collaboration and professional development.
- Potential participation in publications and research presentations.
- Flexible full-time or part-time structure.
- Potential research leadership opportunities as the program expands.