The IMA Group
Join a clinical research team as a Principal Investigator to oversee ongoing and future clinical research studies in a collaborative, patient-centered environment. The role focuses on leading trials, evaluating participants, monitoring safety, and supporting successful trial execution with research staff and site leadership.
Key Responsibilities
- • Lead and oversee clinical trials while ensuring compliance with study protocols and regulatory requirements
- • Screen and evaluate study participants to determine eligibility
- • Monitor participant safety and report adverse events as required
- • Maintain accurate and timely study documentation
- • Collaborate with Sponsors, research staff, and site leadership to support successful trial execution
Required
- • board-certified MD or DO with a background in general medicine and/or metabolic specialties
- • available 2–3 days per week
- • MD or DO with an active, unrestricted medical license
- • Board certification in your specialty
Preferred
- • Prior experience as a Principal Investigator in clinical trials preferred
- • Strong clinical judgment, attention to detail, and communication skills
Benefits & Perks
- • Flexible part-time schedule (2–3 days per week)
- • No nights, weekends, or on-call responsibilities
- • Research-focused role with meaningful patient impact
- • Collaborative, mission-driven team environment
- • 401(k) with employer match
- • Paid time off and holidays
Principal Investigator (MD/DO) – Clinical Research | Part-Time | Austin, TX
IMA Clinical Research is seeking a board-certified MD or DO with a background in general medicine and/or metabolic specialties to join our Austin, TX research team as a Principal Investigator. This is an opportunity to focus on clinical research in a collaborative, patient-centered environment without the demands of traditional clinical practice. We are seeking a physician available 2–3 days per week to provide oversight for ongoing and future clinical research studies. What You'll Do:- Lead and oversee clinical trials while ensuring compliance with study protocols and regulatory requirements
- Screen and evaluate study participants to determine eligibility
- Monitor participant safety and report adverse events as required
- Maintain accurate and timely study documentation
- Collaborate with Sponsors, research staff, and site leadership to support successful trial execution
- MD or DO with an active, unrestricted medical license
- Board certification in your specialty
- Prior experience as a Principal Investigator in clinical trials preferred
- Strong clinical judgment, attention to detail, and communication skills
- Flexible part-time schedule (2–3 days per week)
- No nights, weekends, or on-call responsibilities
- Research-focused role with meaningful patient impact
- Collaborative, mission-driven team environment
- 401(k) with employer match
- Paid time off and holidays
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