Part-Time Principal Investigator — Clinical Research

Site Search Recruitment; Charlotte (NC); Sur place; USD 207 000 - 358 000; Temps partiel

Résumé du poste

Site Search Recruitment is seeking a part-time Principal Investigator 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 from a dedicated research site in the Metrolina region.

Physicians with MD or DO credentials, board certification or eligibility, and an unrestricted license in NC or SC are encouraged to apply.

Qualifications

• MD or DO with board certification or eligibility.
• Active, unrestricted medical license in North Carolina or South Carolina.
• GCP training preferred; training arranged if needed.
• Experience in clinical research is preferred but not required.

Responsabilités

• 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.

Formation

MD or DO, board certified or board eligible

Description du poste

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
• Family medicine and internal medicine
• Endocrinology and obesity medicine

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