Part-Time Principal Investigator — Clinical Research

Summary

Company Overview: Site Search Recruitment works with sites and organizations seeking qualified physician investigators (MD, DO) for roles in clinical research. We are a full-service recruitment and placement firm servicing the research industry.

Job Overview: Our client is seeking a part-time Principal Investigator (PI) to oversee clinical research studies on a flexible, low-time-commitment basis. This role is ideal for a physician or qualified provider looking to supplement their practice with clinical trial work.

Our client has a strong pipeline of studies, and will provide experienced research support staff.

Experienced PIs and sub-investigators are preferred. Physicians new to research are encouraged to apply, particularly in:

• Psychiatry and neurology
• Gastroenterology and hepatology, particularly physicians treating MASH, NASH or fatty liver disease
• Dermatology
• Family medicine and internal medicine
• Endocrinology and obesity medicine
• Rheumatology

Responsibilities

• Serve as Principal Investigator on industry-sponsored clinical trials at a dedicated research site
• Review and confirm participant eligibility
• Perform protocol-required assessments and examinations at key study visits
• Oversee participant safety, including assessment of adverse events
• Supervise delegated study staff and sign off on required study documentation
• Meet with sponsor monitors and support audits and inspections
• Fulfill investigator responsibilities under FDA regulations and ICH Good Clinical Practice

Qualifications

• Research experience is preferred but not required
• GCP certification preferred but not required
• MD or DO, board certified or board eligible required
• Active, unrestricted medical license in North Carolina or South Carolina
• Based in the Metrolina region
• No history of FDA debarment or disqualification, or exclusion from federal healthcare programs
• Willingness to complete Good Clinical Practice (GCP) training, which we arrange

Time, Engagement, and Compensation

• Time: About 3–6 hours a week for each active study during enrollment, and less once enrollment closes.
• Where: At a dedicated research site in the Metrolina region, with study visits scheduled in blocks around your clinic
• Engagement: Independent contractor, under a written investigator agreement
• Compensation: Fee-for-service at fair market value for the study activities you perform. Pay is never tied to referrals or enrollment

Job Description

Company Overview: Site Search Recruitment works with sites and organizations seeking qualified physician investigators (MD, DO) for roles in clinical research. We are a full-service recruitment and placement firm servicing the research industry.

Job Overview: Our client is seeking a part-time Principal Investigator (PI) to oversee clinical research studies on a flexible, low-time-commitment basis. This role is ideal for a physician or qualified provider looking to supplement their practice with clinical trial work.

Our client has a strong pipeline of studies, and will provide experienced research support staff.

Experienced PIs and sub-investigators are preferred. Physicians new to research are encouraged to apply, particularly in:

• Psychiatry and neurology
• Gastroenterology and hepatology, particularly physicians treating MASH, NASH or fatty liver disease
• Dermatology
• Family medicine and internal medicine
• Endocrinology and obesity medicine
• Rheumatology

Responsibilities

• Serve as Principal Investigator on industry-sponsored clinical trials at a dedicated research site
• Review and confirm participant eligibility
• Perform protocol-required assessments and examinations at key study visits
• Oversee participant safety, including assessment of adverse events
• Supervise delegated study staff and sign off on required study documentation
• Meet with sponsor monitors and support audits and inspections
• Fulfill investigator responsibilities under FDA regulations and ICH Good Clinical Practice

Qualifications

• Research experience is preferred but not required
• GCP certification preferred but not required
• MD or DO, board certified or board eligible required
• Active, unrestricted medical license in North Carolina or South Carolina
• Based in the Metrolina region
• No history of FDA debarment or disqualification, or exclusion from federal healthcare programs
• Willingness to complete Good Clinical Practice (GCP) training, which we arrange

Time, Engagement, and Compensation

• Time: About 3–6 hours a week for each active study during enrollment, and less once enrollment closes.
• Where: At a dedicated research site in the Metrolina region, with study visits scheduled in blocks around your clinic
• Engagement: Independent contractor, under a written investigator agreement
• Compensation: Fee-for-service at fair market value for the study activities you perform. Pay is never tied to referrals or enrollment