Jobs at The IMA Group

Conducts evaluation-only medical examinations for disability determinations, including reviewing medical histories and diagnostic testing, performing physical exams, and preparing detailed reports. The role involves no treatment, follow-up care, or on-call responsibilities and requires an active unrestricted MD or DO license and prior clinical experience. The schedule is predictable, with work two Saturdays per month in Spartanburg, South Carolina.

Provide direct clinical supervision and support to patients during dosing sessions for FDA-regulated psychedelic medication trials. Monitors attend recurring dosing visits, complete study-specific training, and support psychiatric investigational studies across PTSD and major depressive disorder indications. The role requires a licensed healthcare provider with graduate-level professional training and psychotherapy experience outside research.

Provides field-based workers’ compensation case management for injured workers. Coordinates medical appointments, care plans, providers, employers, and claims professionals; advocates for patients; supports recovery; and maintains documentation and follow-up. The role serves Los Angeles and surrounding areas, is primarily independent and field-based, and requires extensive travel throughout the assigned territory.

Leads day-to-day operations for a clinical research site, supervising research staff, managing protocol feasibility, budgets, participant activities, regulatory compliance, quality initiatives, SOP development, staffing, and performance reviews. The role also owns study financials, supports site growth, and mentors the clinical research team.

Conduct one-time comprehensive medical evaluations for veterans seeking VA disability benefits. Review medical records, diagnostics, and supporting documentation, then complete detailed disability reports using an electronic platform. The role involves no treatment, prescribing, follow-up care, or on-call responsibilities and is scheduled three days per week.

Conduct one-time medical evaluations for U.S. veterans seeking VA disability benefits. Review medical records, diagnostics, and supporting documentation, then complete detailed disability reports using an electronic platform. This full-time, onsite Physician Assistant role offers a weekday schedule without treatment plans, prescribing, follow-up visits, evenings, weekends, or on-call duties.

Provides field-based workers’ compensation case management for injured workers. Coordinates care among healthcare providers, employers, adjusters, attorneys, and insurers; evaluates treatment plans; attends appointments; facilitates IMEs and job-site assessments; monitors recovery; supports return-to-work planning; and maintains timely clinical documentation.

Coordinates medical care for injured workers throughout Flagstaff and surrounding areas. Attends appointments, collaborates with providers, employers, adjusters, and other stakeholders, monitors treatment and return-to-work plans, identifies recovery barriers, completes clinical documentation, and independently manages a field-based caseload.

Conduct focused physical examinations and review veterans’ medical histories for VA disability evaluations. Document objective findings in a reporting system and submit accurate, timely reports supporting veterans’ claims. The role involves no treatment, prescribing, follow-up care, weekends, or on-call coverage, with a predictable Monday–Friday schedule.

Conduct independent medical evaluations for veterans seeking disability benefits. Perform physical exams, review medical histories and diagnostic records, apply VA disability standards, and prepare objective reports connecting conditions to military service. Submit documentation through a digital case platform in a flexible one- to two-day-per-week schedule, without treatment planning, ongoing patient management, on-call duties, nights, or weekends.

Part-time licensed MD or DO conducting independent medical assessments from an established Gainesville, Georgia office. Responsibilities include clinical interviews, medical record review, accurate electronic documentation, objective report preparation, and communication with support staff. The role offers flexible scheduling, administrative support, and a predictable evaluation-focused workload without hospital coverage, call schedules, or ongoing patient management.

Conduct VA compensation and pension examinations for Veterans, focusing on traumatic brain injury and ENT-related disability evaluations. Review medical records, perform objective assessments, and complete detailed reports according to VA guidelines using an electronic reporting system. The role requires an active unrestricted MD/DO license, clinical physician experience, strong documentation skills, and travel between Pittsburgh and Altoona as needed. It is a flexible, evaluation-only position with no treatment, prescribing, follow-up, or on-call responsibilities.

Serve as Principal Investigator for Phase II-IV clinical trials at a new Augusta research site. Conduct protocol-required medical evaluations, monitor participant safety, assess eligibility, review clinical and regulatory documentation, maintain accurate study records, and communicate with sponsors, CROs, IRBs, and research teams. The role also supports site launch activities, community relationships, regulatory compliance, and adherence to established research workflows. Full-time and part-time schedules are available.

Conduct evaluation-only medical histories and physical examinations for veterans seeking service-connected disability claims. Review diagnostic testing and medical records, prepare VA-compliant reports, and submit evaluations through a digital platform. The role involves no treatment, on-call duties, or follow-up responsibilities.

Performs VA traumatic brain injury disability evaluations one day per week in Syracuse and Watertown. Responsibilities include reviewing medical histories and diagnostics, conducting TBI-focused assessments, and preparing clear, timely reports. The role involves no treatment, follow-ups, nights, weekends, or on-call duties, with potential to expand to full-time by adding general medical examinations.

Conduct comprehensive medical evaluations and physical assessments for Veterans, review histories and diagnostic documentation, and complete accurate clinical reports using established protocols. The physician collaborates with clinical and administrative staff to ensure timely case completion. This office-based role does not involve ongoing treatment, prescribing medication, or long-term patient management, and offers a predictable Monday-Friday daytime schedule without evenings, weekends, or on-call duties.

Leads Phase II–IV clinical trials, ensures protocol and regulatory compliance, evaluates participant eligibility, monitors patient safety, reports adverse events, maintains study documentation, and collaborates with sponsors, research staff, and site leadership. The role requires a board-certified MD or DO with an unrestricted license and prior Principal Investigator experience. It offers a flexible three- to five-day schedule without nights, weekends, or on-call duties.

Serves as Principal Investigator for Phase II-IV psychiatry clinical trials. Responsibilities include evaluating participant eligibility, ensuring protocol and FDA/GCP compliance, monitoring participant safety, overseeing adverse event reporting, maintaining study documentation, and collaborating with sponsors and research staff. The role is part-time, requires an Illinois medical license and psychiatry board certification, and offers $175-$200 per hour.

Serve as Principal Investigator for Phase II-IV clinical trials at a new Louisville research site. Responsibilities include conducting medical evaluations, monitoring participant safety, assessing eligibility, reviewing protocols and regulatory materials, completing study documentation, communicating with sponsors, CROs, and IRBs, and supporting local provider and community relationships.

Serve as Principal Investigator for Phase II-IV clinical trials at a newly launched Cleveland research site. Responsibilities include conducting medical evaluations, monitoring participant safety, assessing eligibility, reviewing protocols and regulatory documentation, completing study records, and coordinating with sponsors, CROs, IRBs, and internal teams. The role also supports community relationship development and adherence to established research workflows and regulatory requirements.