Lead impactful clinical research projects in a dynamic and collaborative environment. Enhance your expertise by overseeing trials and ensuring regulatory compliance. Benefit from comprehensive perks including CME allowance, paid time off, and insurance.
Principal Investigator
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical research activities as a Principal Investigator, ensuring compliance with protocols and regulatory requirements.
- Provide clinical oversight for trials, maintaining participant safety and data integrity.
- Collaborate with multidisciplinary teams to achieve research objectives effectively.
- Conduct study-related procedures including physical exams, informed consent, and adverse event assessments.
- Ensure adherence to FDA regulations, Good Clinical Practice (GCP), and IRB-approved plans.
- Supervise Sub-Investigators and recruitment teams for optimal 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 expert knowledge of study protocols and activities.
- Conduct and supervise research activities in compliance with federal and state regulations.
- Perform subject screening, recruitment, and health assessments as 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 changing 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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