Principal Investigator

Responsibilities include providing clinical oversight, monitoring patient safety, and collaborating with research staff to advance clinical studies. Ideal candidates will have two or more years of clinical experience in family medicine or internal medicine and experience caring for patients presenting with SLD, MASH, and Alzheimer's/Dementia. Candidates must possess strong analytical skills and a dedication to advancing clinical research through high-quality patient care and ethical study practices.The PI assumes overall responsibility for the conduct of the study and agrees to:• Personally conduct or supervise the research• Ensure that each delegated individual is qualified by education, training, and experience• Protect the rights, safety, and welfare of study participantsDuties and Responsibilities• Review and maintain expert knowledge of study-related activities and protocols• Assume all responsibilities and obligations as an Investigator per Title 21 Part 312 and FDA Form 1572• Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times• Maintain sponsor and clinical trial confidentiality• Perform study-related procedures including physical examinations, informed consent, subject history, adverse event review, test article handling, appointment scheduling, records review, treatment coordination, collection of vital signs, and subject health assessments• Review and adjudicate lab, imaging, and biopsy findings• Assist in preparation for study monitor visits• Perform subject screening and recruitment• Provide some weekend coverage to facilitate protocol-required study visits• Provide after-hours phone coverage as neededQualifications• Medical Doctor or DO (active texas license) - clinical research experience preferred but not required• One to two years of clinical practice in Internal Medicine, Family Medicine, Alzheimer’s, Dementia, or Obesity