Psychiatrist - Florida - Clinical Research/Trials - (Up to $375k + Benefits)
Behavioral Health Market Context
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Qualifications
- •M.D. or D.O. degree (required)
- •Board Certification in Psychiatry (or in progress)
- •Active DEA license (or ability to obtain)
- •Active medical license in the State of Florida (or ability to obtain immediately)
- •1–3 years of experience in psychiatric clinical research (Client, Sub-Investigator, or related role)
- •Strong leadership, decision-making, and organizational skills
- •High level of integrity, professionalism, and ethical judgment
- •Excellent interpersonal and communication abilities
- •Ability to interpret clinical data, protocols, and regulatory requirements
- •Detail-oriented with strong documentation and compliance focus
- •7 more items(s)
Responsibilities
- •The Client is responsible for the overall oversight, execution, and integrity of psychiatric clinical trials conducted on behalf of sponsors and pharmaceutical partners
- •This role ensures strict adherence to Good Clinical Practice (GCP), regulatory requirements, and study protocols while safeguarding participant safety and data accuracy
- •The Client collaborates closely with clinical, regulatory, and operational teams to manage study conduct, supervise site personnel, and ensure compliance with federal, state, and sponsor guidelines
- •Evaluate, screen, and enroll study participants based on protocol criteria
- •Conduct psychiatric evaluations, assessments, and physical examinations
- •Monitor participant safety, including identification and management of adverse and serious adverse events
- •Review laboratory results, ECGs, and clinical findings
- •Perform clinical rounds and document patient care as required
- •Provide on-call coverage for study participants when needed
- •Study Execution & Compliance:
- •Ensure studies are conducted in accordance with protocols, GCP, and regulatory standards
- •Maintain compliance with FDA regulations, including Form 1572 requirements
- •Review Investigator’s Brochure prior to study initiation
- •Oversee protocol adherence, including inclusion/exclusion criteria and medication guidelines
- •Ensure proper documentation (electronic and paper) for all study-related activities
- •Evaluate and report safety events, protocol deviations, and non-compliance issues
- •Leadership & Team Management:
- •Delegate study responsibilities appropriately and oversee staff performance
- •Train and certify study personnel on protocol-specific procedures and requirements
- •Review and validate psychiatric rating scales conducted by study raters
- •Collaborate with site leadership to achieve study goals and timelines
- •Regulatory & Administrative Responsibilities:
- •Maintain current CV, licenses, and required credentials
- •Provide documentation to sponsors and IRBs as required
- •Disclose conflicts of interest in accordance with regulations
- •Ensure compliance with patient confidentiality, risk management, and legal standards
- •Maintain accurate and up-to-date study documentation to ensure data integrity
- •Collaboration & Communication:
- •Work closely with sponsors, CROs, and internal teams
- •Attend investigator meetings, training sessions, and educational seminars
- •Travel as needed for study-related meetings
- •Communicate effectively with patients, families, and healthcare professionals
- •Working Hours: Day Shift
- •30 more items(s)
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