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As of Sep 15, 2026, the average hourly pay for international medical graduate doctors in the United States is $41.47, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $51.92 per hour, depending on experience, location, and employer.

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Infographic showing various International Medical Graduate Doctors job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,250 per year, or $41.5 per hour.

International Medical Graduate (IMG) - Clinical Research

Southfield, MI • On-site

Revival Research Institute, LLC
See more jobs at Revival Research Institute, LLCexternal

$22.25 - $29.50/hr

Full-time

Re-posted 23 days ago

Job description

About Revival Research Institute
Revival Research Institute, LLC has been conducting industry-sponsored clinical trials since 2015. Headquartered in Metro Detroit, we operate sites across Michigan, Texas, Illinois, New Jersey, and North Carolina, and have been recognized nationally for the quality of the data we deliver to our sponsors.
About This Role
We are hiring International Medical Graduates with a minimum of 1 year of research experience who can coordinate research visits and maintain study documentation with oversight.
Clinical Research Coordinators at Revival coordinate and manage multiple studies and assist the Principal Investigators and other clinical staff with study-related tasks including, but not limited to:
Responsibilities
  1. Screening, recruitment, and enrollment. Screen, recruit, and enroll research participants. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Collect, process, and ship research specimens, where applicable.
  2. Data and monitoring. Document study-related information in case report forms or electronic data capture systems, handle data queries, and participate in monitoring visits. Obtain, review, and maintain source documents.
  3. Regulatory and quality. Maintain organization of all trial-related documents and correspondence. Implement quality control and assurance methods.
  4. Sponsor and IRB communication. Communicate with study sponsors, the research team, and the Institutional Review Board. Assist with basic regulatory document preparation with oversight, e.g. study amendments, adverse event reporting, protocol deviation reporting.
  5. Professional and technical knowledge. Maintain professional and technical knowledge of clinical trials and standards of care.
  6. Participant confidentiality. Protect patient confidentiality.
Preferred Qualifications
  1. International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.
  2. Minimum of 1 year of research experience.
  3. Radiology experience is preferred. Phlebotomy skills are also preferred.
  4. Database and computer skills: Microsoft Office (Word, Excel), Outlook; excellent verbal and written communication skills; ability to work independently and assume responsibility; excellent organizational skills; ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff, and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.

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