Principal Investigator

in Healthcare + Life Sciences
  • Edinburg, Texas View on Map
  • Salary: $240,000.00 - $25,000.00
Permanent

Job Detail

  • Experience Level Principal
  • Degree Type Doctor of Philosophy (PhD)
  • Employment Full Time
  • Working Type On Site
  • Job Reference 0000015961
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    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.

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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