Psychiatrist – Clinical Research (Sub-Investigator / Investigator Track) / Miami Lakes, FL (Up to 400k + Based on Exp.)

Benefits

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)
• •Skills: Strong clinical judgment and decision-making 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
• •6 more items(s)

Responsibilities

• •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
• •On-call responsibilities may be required
• •Travel for investigator meetings or study-related activities as needed
• •Fast-paced, collaborative clinical research environment
• •Job Responsibilities: Clinical Oversight & Patient Care
• •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
• •Working Hours: Monday – Friday, standard business hours (8:00 AM – 5:00 PM)
• •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
• •27 more items(s)