Principal Investigator
125 an hour
Behavioral Health Market Context
Apply Nowvia Green Key Resources
Job Description
atory 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.
• 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.
Qualifications
- •Doctor of Philosophy (PhD) with a background in Internal or Family Medicine
- •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
Benefits
Responsibilities
- •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
- •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
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