Serve as Principal Investigator overseeing impactful clinical research studies. Collaborate with multidisciplinary teams ensuring compliance and participant safety. Enhance your expertise in a dynamic, research-focused environment.
Principal Investigator
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical research studies and oversee trial protocols as Principal Investigator.
- Ensure compliance with regulatory requirements and ethical standards in research.
- Collaborate with multidisciplinary teams to manage study-related activities.
- Provide clinical expertise and supervision for research participants' safety and welfare.
- Conduct and supervise study procedures, including informed consent and data collection.
- Maintain confidentiality and integrity of research data and findings.
- Adhere to Good Clinical Practice (GCP) and FDA regulations throughout research.
- Contribute to the preparation for study monitor visits and audits.
- Facilitate subject recruitment and screening processes for clinical trials.
Key Responsibilities & Duties
- Supervise and conduct clinical research studies adhering to approved protocols.
- Ensure all delegated tasks are performed by qualified personnel.
- Protect participants' rights, safety, and welfare during research activities.
- Review and adjudicate laboratory, imaging, and biopsy findings.
- Provide clinical oversight and support for study-related procedures.
- Maintain compliance with federal, state, and institutional regulations.
- Participate in recruitment and screening of study participants.
- Collaborate with sub-investigators and recruitment teams to meet study goals.
- Provide weekend and after-hours coverage as required by study protocols.
Job Requirements
- Doctor of Medicine (MD) with active Texas physician license.
- Board certification in Family Medicine, Internal Medicine, or Hepatology preferred.
- Minimum two years of clinical practice experience in relevant fields.
- Prior clinical research experience as Principal Investigator preferred.
- Proficiency in English; Spanish fluency strongly preferred.
- Strong organizational, communication, and interpersonal skills.
- Knowledge of GCP, FDA regulations, and clinical trial protocols.
- Ability to work in clinical and laboratory environments with protective equipment.
- Experience with Microsoft Office and web-based enterprise solutions.
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