Lead groundbreaking clinical research projects ensuring compliance and innovation. Collaborate with multidisciplinary teams to enhance participant safety and data integrity. Enjoy comprehensive benefits including CME allowance, paid time off, and insurance.
Principal Investigator
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical research initiatives as a Principal Investigator, ensuring adherence to protocols and regulatory standards.
- Provide expert oversight for clinical trials, prioritizing participant safety and data accuracy.
- Collaborate with multidisciplinary teams to achieve research objectives and drive innovation.
- Conduct study-related procedures, including physical exams, informed consent, and adverse event evaluations.
- Ensure compliance with FDA regulations, Good Clinical Practice (GCP), and IRB-approved protocols.
- Supervise Sub-Investigators and recruitment teams to optimize study execution.
- Maintain confidentiality of study sponsors and clinical trial data at all times.
- Provide weekend and after-hours coverage as needed to support study protocols.
Key Responsibilities & Duties
- Review and maintain comprehensive knowledge of study protocols and activities.
- Conduct and oversee research activities in compliance with federal and state regulations.
- Perform subject screening, recruitment, and health assessments per study requirements.
- Ensure the accuracy, security, and integrity of research data and analysis.
- Coordinate study-related procedures, including lab reviews, imaging, and biopsy findings.
- Prepare for and participate in study monitor visits and audits.
- Provide clinical support and oversight for trial participants, ensuring their safety and welfare.
- Collaborate with teams to adapt to evolving priorities and ensure study success.
Job Requirements
- Doctor of Philosophy (PhD) in a relevant field required.
- Minimum of 2 years of clinical experience; research experience preferred.
- Current physician license in Texas; board certification preferred.
- Proficiency in English and Spanish strongly preferred.
- Strong knowledge of FDA regulations, GCP, and clinical trial protocols.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work in a clinical environment with exposure to biological fluids.
- Proficiency in Microsoft Office and web-based enterprise solutions software.
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