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Foreign Medical Jobs (NOW HIRING)

ECare Medical Group

Foreign Medical Graduate

Houston, TX · On-site

$16.50 - $21/hr

Job Details: * Physician who received a basic medical degree from a medical school located outside the United States and Canada that is not accredited by a U.S. accrediting body, the Liaison ...

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How much do foreign medical jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for foreign medical in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $21.15 per hour, depending on experience, location, and employer.

What are Foreign Medical graduates?

Foreign Medical graduates are individuals who have completed their medical education outside the country in which they intend to practice medicine. These graduates often need to go through additional certification, exams, or training to meet the licensing requirements of their desired country. In the United States, for example, foreign medical graduates must pass the United States Medical Licensing Examination (USMLE) and obtain certification from the Educational Commission for Foreign Medical Graduates (ECFMG) before applying for residency or medical practice. The process ensures that all practicing physicians meet the same standards of medical knowledge and skills.

What are the key skills and qualifications needed to thrive as a Foreign Medical Graduate, and why are they important?

To thrive as a Foreign Medical Graduate, you need a recognized medical degree, passing scores on relevant licensing exams (such as USMLE for the U.S.), and clinical experience in your target country. Familiarity with healthcare systems, electronic health records, and language proficiency tests (like TOEFL or IELTS) is often required. Strong adaptability, cultural sensitivity, and effective communication skills help you collaborate with diverse patients and medical teams. These competencies are crucial for ensuring patient safety, delivering quality care, and successfully integrating into a new healthcare environment.

What challenges might a foreign medical graduate face when integrating into a new healthcare system?

Foreign medical graduates often encounter challenges such as adapting to different clinical protocols, communication styles, and regulatory requirements in a new country. Navigating licensing exams, understanding local healthcare laws, and building professional networks can also be demanding. However, many institutions offer orientation programs, mentorship, and support resources to help ease the transition and promote professional growth. Being proactive in seeking guidance and participating in continuous education can greatly enhance integration and success.
What cities are hiring for Foreign Medical jobs? Cities with the most Foreign Medical job openings:
What states have the most Foreign Medical jobs? States with the most job openings for Foreign Medical jobs include:
Foreign Medical jobs near you
Infographic showing various Foreign Medical job openings in the United States as of June 2026, with employment types broken down into 15% As Needed, 23% Full Time, and 62% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $40,170 per year, or $19.3 per hour.
Foreign Medical Graduate

Foreign Medical Graduate

DM Clinical Research

New York, NY

Full-time

Posted 28 days ago

Job description

Foreign Medical Graduate (FMG)

The Foreign Medical Graduate (FMG) will take on our Clinical Research Coordinator III role in New Jersey. The FMC will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor at our site located in New Jersey. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES amp; RESPONSIBILITIES
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training, as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
  • Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
  • Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
  • Ability to train and mentor site staff, as needed
  • Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
  • Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
  • Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
  • Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings
  • Any other matters as assigned by management
KNOWLEDGE amp; EXPERIENCE
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree preferred
  • Foreign Medical Graduates preferred
Experience:
  • Minimum of 5 years experience in Clinical Research
  • Supervisory experience preferred
  • Wide therapeutic range of clinical trials experience preferred
  • Regulatory research experience is a plus
Credentials:
  • ACRP or equivalent certification is preferred
Knowledge and Skills:
  • Goals-driven while continuously maintaining quality.
  • Must be detailed-oriented, proactive, and able to take initiative.
  • Must have strong written and communication skills.
  • Must have excellent customer service skills.
  • Bilingual in Spanish is a plus

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