Principal Investigator – Psychiatrist

Overview

• Lead clinical trial activities ensuring compliance with FDA, ICH, and GCP guidelines.
• Provide medical oversight and ensure participant safety during trials.
• Collaborate with local and central teams to enhance study quality.
• Evaluate participants for eligibility and oversee enrollment processes.
• Engage in participant retention strategies and ensure protocol adherence.
• Participate in investigator meetings and ongoing education activities.
• Ensure accurate data recording and compliance with HIPAA guidelines.
• Maintain professional interactions with sponsors, clients, and team members.

Key Responsibilities & Duties

• Conduct clinical trials adhering to ethical and regulatory standards.
• Evaluate and assess participants for trial eligibility.
• Provide oversight to ensure participant safety and protocol compliance.
• Collaborate with teams to enhance site efficiency and study quality.
• Participate in training sessions and investigator meetings.
• Ensure accurate and detailed documentation of trial data.
• Maintain compliance with HIPAA and other regulatory guidelines.
• Adapt to workload changes and prioritize tasks effectively.

Job Requirements

• Doctoral degree (MD or DO) with active physician license in good standing.
• Board certification in Psychiatry is mandatory.
• Proficiency in clinical procedures and computer applications like MS Office.
• Strong organizational skills and attention to detail.
• Effective written and verbal communication skills; bilingual proficiency preferred.
• Ability to handle sensitive information confidentially and professionally.
• Self-motivated with a strong work ethic and adaptability.
• Experience in clinical trials and regulatory compliance.