Psychiatrist – Clinical Research (Sub-Investigator / Investigator Track) / Miami Lakes, FL (Up to 400k + Based on Exp.)
Updated 10/06/26
$300,000
– $400,000
yearly
33016, Hialeah, Florida, United States
Physician
Psychiatry-Consultation Liaison
By applying you agree to our Terms of Service
Job at a glance
Degree Required
MD/DO
Position Type
Full-Time
Work Environment
Clinic/Private Practice
Outpatient
Visa Sponsorship
No
Experience Level
2 years
Job description
Job description
Psychiatrist – Clinical Research (Sub-Investigator / Investigator Track)
📍 Miami Lakes, FL
💰 Competitive Compensation + Benefits
🕒 Full-Time | Clinical Research Setting
Overview
We are seeking a Board-Certified or Board-Eligible Psychiatrist to join a growing clinical research team in Miami Lakes, Florida.
This role offers a unique opportunity to work at the intersection of psychiatry and clinical research, supporting cutting-edge studies while maintaining a strong focus on patient safety, data integrity, and regulatory compliance.
You will collaborate with sponsors, CROs, and multidisciplinary clinical teams to ensure high-quality study execution in a fast-paced, research-driven environment.
Additional Details
- On-call responsibilities may be required
- Travel for investigator meetings or study-related activities as needed
- Fast-paced, collaborative clinical research environment
Why Join This Opportunity?
- Be part of innovative psychiatric clinical trials
- Work alongside experienced research professionals and sponsors
- Contribute to advancing new treatments in mental health
- Growth opportunities within clinical research leadership
If you’re a Psychiatrist interested in clinical research, innovation, and patient-centered care, we’d love to connect.
Job Responsibilities
Evaluate, screen, and enroll study participants based on protocol criteria
Conduct psychiatric evaluations, assessments, and physical exams
Monitor patient safety, including adverse and serious adverse events
Review labs, ECGs, and clinical findings
Provide on-call coverage for study participants as needed
Study Execution & Compliance
Ensure studies are conducted in accordance with GCP, FDA regulations, and study protocols
Maintain compliance with regulatory requirements, including Form 1572
Review Investigator’s Brochure and protocol requirements
Oversee inclusion/exclusion criteria and medication compliance
Document and report safety events, protocol deviations, and compliance issues
Leadership & Team Collaboration
Delegate and oversee study responsibilities across clinical staff
Train and support site personnel on protocol-specific procedures
Review and validate psychiatric rating scales
Partner with leadership to meet study timelines and performance goals
Regulatory & Administrative Responsibilities
Maintain current licensure, credentials, and documentation
Provide required documentation to sponsors and IRBs
Ensure compliance with patient confidentiality and regulatory standards
Maintain accurate and complete study documentation
Qualifications
M.D. or D.O. (Required)
Board Certified or Board Eligible in Psychiatry
Active DEA license (or ability to obtain)
Active Florida medical license (or ability to obtain immediately)
Experience
1–3 years of clinical research experience preferred (Investigator, Sub-Investigator, or similar role)
Experience working in GCP/FDA-regulated environments preferred
Working Hours
No traditional hospital call; however, light on-call coverage may be required for study participants (protocol-dependent)
Schedule may vary slightly based on study visits, patient volume, and sponsor timelines
Skills
High level of professionalism and ethical standards
Excellent communication and patient interaction skills
Ability to interpret clinical protocols and regulatory requirements
Detail-oriented with strong documentation and compliance focus
By applying you agree to our Terms of Service