Principal Investigator

Principal Investigator Overview

• The Principal Investigator will lead clinical research initiatives at a newly launched site in California.
• This full-time role involves conducting and supervising clinical trials in the SLD and cardiometabolic domains.
• Responsibilities include ensuring compliance with federal regulations, IRB protocols, and company policies.
• Relocation support of $25,000 is available, paid after the initial hire period.
• The position offers a dynamic environment with exposure to innovative clinical research methodologies.
• Ideal candidates will have strong expertise in Steatotic Liver Disease (SLD) and cardiometabolic research.
• Work involves collaboration with sub-investigators and recruitment teams to ensure study success.
• The role requires flexibility to adapt to changing priorities and provide weekend coverage as needed.
• Candidates must possess excellent communication skills and a professional demeanor.

Principal Investigator Key Responsibilities & Duties

• Conduct and oversee clinical trials, ensuring adherence to protocols and regulatory requirements.
• Supervise delegated tasks, ensuring team members are qualified and trained.
• Protect participant rights, safety, and welfare throughout the research process.
• Perform study-related procedures including physical exams, informed consent, and health assessments.
• Review and adjudicate laboratory, imaging, and biopsy findings for accuracy.
• Manage subject screening, recruitment, and scheduling to meet study goals.
• Provide after-hours phone coverage and weekend support for study visits.
• Ensure confidentiality of study sponsor and clinical trial information.
• Collaborate with teams to prepare for study monitor visits and audits.

Principal Investigator Job Requirements

• Doctor of Medicine (MD) degree with at least 5 years of clinical research experience.
• Prior experience as a Principal Investigator in SLD or cardiometabolic research.
• Proficiency in FDA regulations, Good Clinical Practice (GCP), and IRB protocols.
• Strong organizational skills and attention to detail in managing clinical trials.
• Bilingual proficiency in English and Spanish is strongly preferred.
• Excellent computer skills, including proficiency in Microsoft Office and web-based enterprise solutions.
• Ability to work on-site in a clinical environment with exposure to biological fluids.
• Flexibility to provide weekend and after-hours coverage as needed.
• Strong interpersonal skills and a professional demeanor to collaborate effectively.