Principal Investigator

Overview

• Lead clinical research studies as Principal Investigator, ensuring compliance with protocols and ethical standards.
• Collaborate with multidisciplinary teams to oversee study-related activities and participant safety.
• Provide clinical expertise and supervision for research participants' welfare and data integrity.
• Ensure adherence to Good Clinical Practice (GCP) and regulatory guidelines throughout research processes.
• Contribute to the preparation and execution of study monitor visits and audits.
• Facilitate participant recruitment and screening for clinical trials, ensuring diversity and inclusion.
• Maintain confidentiality and integrity of research data and findings.
• Engage in continuous learning to stay updated on advancements in clinical research methodologies.

Key Responsibilities & Duties

• Supervise and conduct clinical research studies, ensuring adherence to approved protocols and ethical standards.
• Oversee delegated tasks, ensuring they are performed by qualified personnel.
• Protect participants' rights, safety, and welfare during all research activities.
• Review and adjudicate laboratory, imaging, and biopsy findings with precision.
• Provide clinical oversight and support for study-related procedures and data collection.
• Ensure compliance with federal, state, and institutional regulations governing clinical trials.
• Collaborate with sub-investigators and recruitment teams to meet study objectives effectively.
• Participate in recruitment and screening processes to ensure participant eligibility and diversity.
• Provide weekend and after-hours coverage as required by study protocols.

Job Requirements

• Doctor of Medicine (MD) with an active physician license.
• Board certification in Family Medicine, Internal Medicine, or Hepatology preferred.
• Minimum two years of clinical practice experience in relevant medical fields.
• Prior experience as Principal Investigator in clinical research is highly desirable.
• Proficiency in English; Spanish fluency is strongly preferred for participant communication.
• Strong organizational, communication, and interpersonal skills for effective team collaboration.
• Knowledge of GCP, FDA regulations, and clinical trial protocols is essential.
• Ability to work in clinical and laboratory environments with necessary protective equipment.
• Proficiency in Microsoft Office and web-based enterprise solutions for documentation and reporting.