Principal Investigator – Internal Medicine

Overview

• Lead clinical trial activities ensuring compliance with FDA, ICH, and GCP guidelines.
• Oversee participant safety and ethical execution of clinical studies.
• Collaborate with local and central teams to ensure study quality.
• Evaluate and enroll eligible participants in clinical trials.
• Engage in protocol training and continuing education activities.
• Ensure accurate data recording and adherence to protocol guidelines.
• Participate in Investigator Meetings and recruitment affairs.
• Maintain confidentiality and professionalism in handling sensitive information.

Key Responsibilities & Duties

• Conduct clinical trials following FDA, ICH, NIH, and GCP guidelines.
• Provide site leadership to enhance efficiency and compliance.
• Assess participant eligibility and ensure safety during trials.
• Collaborate with sponsors, clients, and team members effectively.
• Train staff on protocols and ensure adherence to study requirements.
• Engage in participant retention and successful study delivery.
• Handle multiple tasks and adapt to workload changes efficiently.
• Identify problems and implement solutions independently.

Job Requirements

• MD or DO degree with active physician license in good standing.
• Board certification in area of specialty and clinical trial experience.
• Proficiency in MS Office, electronic health records, and web applications.
• Strong organizational, communication, and interpersonal skills.
• Bilingual proficiency in English and Spanish is highly preferred.
• Ability to handle sensitive information confidentially and professionally.
• CPR certification required; ACLS certification preferred.
• Self-motivated with a strong work ethic and adaptability.