Clinical Research Principal Investigator (MD or DO Only -All Specialties Welcome

Clinitiative Health Research; Town of Texas (WI); Remote; USD 100,000 - 125,000; Part time

Job summary

A research organization is seeking a Clinical Research Principal Investigator to oversee flexible, compensated trial opportunities with minimal administrative interaction. Ideal for physicians looking to enhance their medical contributions while maintaining clinical autonomy. Training and matching based on specialty are provided, making this a unique opportunity to participate in clinical research without prior experience.

Benefits

Flexible schedule

Minimal administrative work

Malpractice insurance covered

Qualifications

• Must be a board-certified physician.
• Willingness to undertake training and mentorship.
• Flexibility in working hours is essential.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator.
• Conduct study visits aligned with clinical duties.
• Ensure compliance with protocol and regulatory requirements.

Skills

Clinical research experience

Patient care

Protocol compliance

Collaboration

Education

M.D., D.O, or equivalent doctoral-level degree

Active, unrestricted medical license

Board certification in specialty

Job description

Overview

Clinical Research Principal Investigator (MD or DO Only – All Specialties Welcome)
Remote Matching · Contract · Dallas, Texas, United States

Are you a hospitalist, private practice physician, or existing principal investigator looking to supplement your income and contribute to medical innovation—without adding administrative burden or sacrificing your clinical autonomy? Join Clininitiative Health Research's ClinPI Program, a nationwide initiative that matches board-certified physicians with local, flexible clinical trial opportunities based on your specialty and availability.

No research experience required. We provide full training, mentorship, and support.

Opportunity Highlights

• Flexible schedule: Set your own hours (typically 5–10+ hours/week)
• Local studies only: Opportunities are based in the city where you currently live or practice
• Minimal administrative work: Site staff manages study paperwork
• Standard-of-care clinical work: No procedures outside typical patient care within the protocol
• Malpractice covered: No additional insurance needed—you are indemnified by the sponsor
• Study durations: Trials typically last 3 to 12 months
• Tailored matching: You will be matched with trials aligned with your specialty and clinical interests

The Process

1. Apply online
2. Complete your physician career profile (medical background, specialty, clinical preferences)
3. Upon approval, you are registered into the ClinPI Program
4. You will receive portal access where you can:

• Register for our clinical research training course
• View available trials in your area
• Apply to studies that fit your interests, specialty, and time availability

Once matched, we will connect you with the participating research site for onboarding and trial initiation.

Role Responsibilities

• Serve as a Principal Investigator (PI) or Sub-Investigator on studies
• Conduct study visits aligned with standard-of-care clinical duties
• Ensure compliance with protocol and regulatory requirements
• Collaborate with study coordinators and site teams
• Maintain GCP standards (certification provided if not already completed)

Who This Is For

• Hospitalists, private practice physicians, or locum providers seeking flexible supplemental income
• Clinicians curious about research but unsure where to start
• Physicians wanting to advance medicine while maintaining their clinical independence

Join ClinPI to explore the clinical research world without making a career shift. This is not a job posting for one role—it is a gateway to a steady stream of vetted, compensated trial opportunities, with no cost to join.

Apply now to unlock your earning potential in research and take the first step toward becoming a Principal Investigator.

• M.D., D.O, or equivalent doctoral-level degree
• Active, unrestricted medical license in your state
• Board certification in your specialty
• Willingness to see patients at a designated research site
• No prior research experience required—training and mentorship provided