Principal Investigator

Overview

• Lead clinical trial activities ensuring compliance with ICH/FDA/GCP guidelines and local regulations.
• Provide medical oversight to ensure participant safety and ethical execution of trials.
• Collaborate with local and central teams to drive study quality and efficiency.
• Evaluate participant eligibility and ensure proper enrollment in trials.
• Engage in participant retention and successful delivery of study objectives.
• Participate in protocol training and investigator meetings to maintain knowledge.
• Ensure adherence to HIPAA guidelines and maintain confidentiality of sensitive information.
• Adapt to workload changes and prioritize tasks effectively.

Key Responsibilities & Duties

• Conduct clinical trial activities following established guidelines and protocols.
• Ensure participant safety and ethical execution of trials.
• Provide leadership to enhance site efficiency and compliance.
• Evaluate and assess participant eligibility for trial enrollment.
• Collaborate with sponsors, clients, and team members positively.
• Record data accurately and ensure protocol adherence.
• Participate in training sessions to maintain protocol knowledge.
• Handle sensitive information professionally and confidentially.

Job Requirements

• Doctoral degree (MD or DO) with active physician license in good standing.
• Board certification in Dermatology is required.
• Proficiency in clinical procedures and computer applications.
• Strong organizational and communication skills, with attention to detail.
• Ability to adapt to workload changes and prioritize effectively.
• Bilingual proficiency in English and Spanish is highly preferred.
• Ability to handle sensitive information confidentially and professionally.
• Self-motivated with a strong work ethic and urgency.