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International Medical Program Coordinator Jobs (NOW HIRING)

Integrated 3D

Program Coordinator

Redmond, OR · On-site

$32 - $36/hr

Compensation includes: * 100% employer paid Medical, Dental and Vision for Employee (includes ... Compliant with the International Traffic in Arms Regulations (ITAR) which requires U.S. person ...

The Salvation Army

Program Coordinator

Hoffman Estates, IL · On-site

$23 - $25/hr

About The Salvation Army The Salvation Army, an international movement, is an evangelical part of ... Medical, prescription drug, dental, vision, and hearing coverage * Employer-paid basic life and AD ...

MUSC

Program Coordinator

Charleston, SC · On-site

Entity Medical University Hospital Authority (MUHA) Worker Type Employee Worker Sub-Type​ Regular ... The Program Coordinator - Case Management reports to the Manager of Case Management. Under general ...

voagny

Program Coordinator

Manhattan, NY

Position: Program Coordinator The CEEP Program Coordinator is responsible for the day-to-day ... Medical, Dental, & Vision Coverage * Prescription Coverage * Life Insurance * Retirement Plan

Avispa Technology

Program Coordinator

Stanford, CA · Remote

$40/hr

W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL * 40 hours/week, 6 Month Assignment A leading university is seeking a Program Coordinator to support industry ...

Northwestern University

Program Coordinator

Evanston, IL · On-site

$53K - $68K/yr

This role supports the Roberta Buffett International Studies Program by fostering undergraduate ... and holidays; paid medical/sick and parental leave; tuition benefits for the employee and ...

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International Medical Program Coordinator information

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How much do international medical program coordinator jobs pay per year?

As of Sep 11, 2026, the average yearly pay for international medical program coordinator in the United States is $67,070.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $70,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to International Medical Program Coordinator jobs?

For International Medical Program Coordinator jobs, the most frequently searched job titles are:

Infographic showing various International Medical Program Coordinator job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $67,070 per year, or $32.2 per hour.

International Medical Graduate (IMG) - Clinical Research Coordinator

Denton, TX • On-site

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

$22.75 - $30.25/hr

Full-time

Re-posted 14 days ago

Job description

Unique opportunity to make an Impact in the healthcare industry… 

Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, North Carolina, New Jersey. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.  

As Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.  

We are seeking International Medical Graduates with a minimum of 3 year of research experience and a strong interest in the Clinical Research field would be an excellent fit for our position. Our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.  

New Staff should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Some responsibilities will include coordinating and managing multiple studies. They are also responsible for assisting the Principal Investigators and other clinical staff, with any study related tasks as follows but not limited to: 

  1. Research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable. 

  2. Document study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents. 

  3. Maintain organization of all trial related documents and correspondence. Implement quality control and assurance methods. 

  4. Communicate with study sponsors, 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. Maintain professional and technical knowledge of Clinical trials and Standards of Care. 

  6. Protect patient confidentiality. 

Preferred Qualifications 

  1. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg

  2. Radiology experience is preferred. Phlebotomy skills are also preferred.  

  3. Additional Qualifications: 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. 

JOIN US & GROW YOUR KNOWLEDGE & EXPERIENCE!!! 

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