Lead impactful clinical research projects advancing cardiometabolic and MASLD/MASH studies. Collaborate with multidisciplinary teams in a dynamic, on-site environment. Enhance your expertise in clinical trial management.
Principal Investigator
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Principal Investigator Overview
- The Principal Investigator oversees clinical research activities, ensuring compliance with regulations and ethical standards.
- This full-time role involves dual-site coverage focused on cardiometabolic and MASLD/MASH research.
- Collaborate with multidisciplinary teams to conduct and supervise clinical trials effectively.
- Ensure participant safety and data integrity throughout the research process.
- Provide clinical support and oversight for study protocols and activities.
- Maintain confidentiality and adhere to Good Clinical Practice (GCP) guidelines.
- Offer expert knowledge and leadership in clinical trial operations and management.
- Contribute to advancing medical research and improving patient outcomes.
Principal Investigator Key Responsibilities & Duties
- Conduct and supervise clinical research activities, ensuring adherence to protocols and regulations.
- Oversee participant recruitment, screening, and informed consent processes.
- Perform study-related procedures, including physical exams and health assessments.
- Ensure the accuracy, security, and integrity of research data and analysis.
- Collaborate with sub-investigators and recruitment teams to meet study objectives.
- Provide after-hours coverage and weekend support as needed for study visits.
- Prepare for and facilitate study monitor visits and audits.
- Maintain compliance with federal, state, and organizational policies and standards.
Principal Investigator Job Requirements
- Doctor of Medicine (MD) degree with a minimum of 5 years of clinical experience.
- Previous experience as a Principal Investigator preferred but not required.
- Proficiency in written and oral communication; bilingual in English and Spanish preferred.
- Strong organizational skills and attention to detail in clinical trial operations.
- Knowledge of FDA regulations, GCP guidelines, and IRB protocols.
- Ability to work on-site in clinical and laboratory environments with protective equipment.
- Proficiency in Microsoft Office and web-based enterprise solutions software.
- Strong interpersonal skills and a professional demeanor in team collaboration.
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