Lead impactful clinical research projects in a dynamic, innovative environment. Collaborate with multidisciplinary teams and advance medical knowledge through research. Enjoy professional growth and competitive benefits in this rewarding role.
Principal Investigator
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Serve as Principal Investigator overseeing clinical research activities and ensuring compliance with federal regulations and protocols.
- Conduct clinical trials, supervise research staff, and ensure participant safety and data integrity.
- Collaborate with multidisciplinary teams to advance clinical research initiatives and outcomes.
- Provide expert knowledge in study protocols, regulatory requirements, and Good Clinical Practice (GCP).
- Perform study-related procedures including physical examinations, informed consent, and adverse event monitoring.
- Ensure the accuracy, security, and integrity of research data and analysis.
- Support recruitment efforts and oversee sub-investigators and research teams.
- Participate in sponsor visits and provide after-hours coverage as needed.
Key Responsibilities & Duties
- Conduct and supervise clinical research activities in compliance with regulatory standards and protocols.
- Maintain confidentiality of study sponsor and clinical trial information.
- Perform subject screening, recruitment, and health assessments per study protocols.
- Ensure proper delegation and oversight of tasks to qualified research staff.
- Monitor and adjudicate lab, imaging, and biopsy findings for study participants.
- Prepare for and participate in study monitor visits and audits.
- Provide weekend and after-hours coverage to facilitate study visits as required.
- Oversee and mentor sub-investigators and recruitment teams to ensure study success.
Job Requirements
- Doctor of Philosophy (PhD) with a background in Internal or Family Medicine.
- Minimum of 2 years clinical experience; 3 years preferred.
- Current physician license in Texas; board certification preferred.
- Proficiency in Spanish strongly preferred for effective communication.
- Strong organizational and interpersonal skills with attention to detail.
- Knowledge of FDA regulations, GCP, and clinical research protocols.
- Experience with Microsoft Office and web-based enterprise solutions software.
- Ability to work in clinical environments with exposure to biological fluids and pathogens.
- ShareAustin: