Principal Investigator (MD/DO) - Part-Time
Waco, TXPart-time
Behavioral Health Market Context
Apply Nowvia Paylocity
Job Description
ransforming how research is conducted at the point of care. Using our proprietary technology, we aim to:
• Increase patient access to research trials within our communities
• Provide physicians with enhanced care options for current patients
• Deliver superior clinical research enrollment metrics to Pharma sponsors
All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.
Key Responsibilities:
• Serve as the Principal Investigator for assigned clinical trials, ensuring overall study oversight.
• Oversee and enforce compliance with study protocols while prioritizing subject safety at all times.
• Conduct and document physical examinations and medical assessments in accordance with research protocol requirements.
• Provide continuous medical oversight throughout all phases of the clinical trial lifecycle.
• Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution.
• Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed.
• Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs.
Qualifications:
• MD or DO with a valid and active medical license in the state of Texas with no history of license suspension or disbarment.
• Board certification in Internal Medicine or Family Medicine (additional specialty certifications are welcome).
• Prior clinical research experience is preferred but not required.
• Strong attention to detail and a demonstrated commitment to high ethical standards.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively in a team-based environment.
Requirements
This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant
• Increase patient access to research trials within our communities
• Provide physicians with enhanced care options for current patients
• Deliver superior clinical research enrollment metrics to Pharma sponsors
All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.
Key Responsibilities:
• Serve as the Principal Investigator for assigned clinical trials, ensuring overall study oversight.
• Oversee and enforce compliance with study protocols while prioritizing subject safety at all times.
• Conduct and document physical examinations and medical assessments in accordance with research protocol requirements.
• Provide continuous medical oversight throughout all phases of the clinical trial lifecycle.
• Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution.
• Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed.
• Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs.
Qualifications:
• MD or DO with a valid and active medical license in the state of Texas with no history of license suspension or disbarment.
• Board certification in Internal Medicine or Family Medicine (additional specialty certifications are welcome).
• Prior clinical research experience is preferred but not required.
• Strong attention to detail and a demonstrated commitment to high ethical standards.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively in a team-based environment.
Requirements
This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant
Qualifications
- •MD or DO with a valid and active medical license in the state of Texas with no history of license suspension or disbarment
- •Board certification in Internal Medicine or Family Medicine (additional specialty certifications are welcome)
- •Strong attention to detail and a demonstrated commitment to high ethical standards
- •Excellent communication and interpersonal skills, with the ability to collaborate effectively in a team-based environment
- •This job requires legal authorization to work in the US
Benefits
Responsibilities
- •This is a unique opportunity for a physician in Internal Medicine or Family Medicine to contribute to innovative clinical research while maintaining a flexible schedule
- •Provide physicians with enhanced care options for current patients
- •Deliver superior clinical research enrollment metrics to Pharma sponsors
- •All with the ultimate goal of Improving Patient Outcomes at the Point of Care
- •Serve as the Principal Investigator for assigned clinical trials, ensuring overall study oversight
- •Oversee and enforce compliance with study protocols while prioritizing subject safety at all times
- •Conduct and document physical examinations and medical assessments in accordance with research protocol requirements
- •Provide continuous medical oversight throughout all phases of the clinical trial lifecycle
- •Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution
- •Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed
- •Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs
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