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Foreign Medical Graduate Research Jobs (NOW HIRING)

Horizon Clinical Research

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Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Are you a foreign medical graduate? Education: * Bachelor's (Preferred) Experience: * Clinical research: 1 year (Preferred) Work Location: In person

Fermilab

Graduate Research Assistant

Batavia, NY · On-site

$20 - $35/hr

What Your Day-to-Day as a Graduate Research Assistant at Fermilab Will Look Like: * Perform ... Foreign Government Sponsored Activities Fermilab employees, and certain guest researchers and ...

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Essen Medical Associates

Clinical Assistant

Bronx, NY · On-site

$16 - $18/hr

Clinical Assistant/ Foreign Medical Graduate Required The Clinical Assistant plays a vital role in supporting healthcare providers in delivering high-quality, personalized care to patients.

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How much do foreign medical graduate research jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for foreign medical graduate research in the United States is $43.97, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $53.37 per hour, depending on experience, location, and employer.

What are typical career advancement opportunities for foreign medical graduate research?

Foreign Medical Graduate Researchers often begin in research assistant or associate roles, gaining experience in designing studies, analyzing data, and publishing findings. With continued professional development and successful research outcomes, advancement can lead to senior researcher, project lead, or principal investigator positions, and, in some cases, transition into clinical or academic roles. Many researchers further their careers by obtaining additional certifications or advanced degrees, such as a PhD or MPH. The field offers opportunities to specialize, collaborate with international research teams, and contribute to advancements in global health.

What is a foreign medical graduate research?

A Foreign Medical Graduate (FMG) Research job involves conducting clinical or laboratory research in healthcare or medical sciences, typically in academic institutions, hospitals, or research centers. FMGs in these roles assist in data collection, analysis, manuscript preparation, and clinical trials. This position helps FMGs gain experience in the U.S. healthcare system, build professional networks, and improve their credentials for residency applications. Many FMG research roles require strong analytical skills, medical knowledge, and sometimes prior research experience.

What are the key skills and qualifications needed to thrive in foreign medical graduate research?

To thrive as a Foreign Medical Graduate Researcher, a strong background in medical sciences, research methodology, and often an MD or equivalent degree is essential. Familiarity with data analysis tools such as SPSS or R, scientific databases like PubMed, and research ethics certification (e.g., CITI) are commonly required. Excellent written and verbal communication, adaptability, and critical thinking distinguish top performers in this role. These skills ensure the ability to design, conduct, and communicate high-quality research, contributing effectively to multidisciplinary medical teams.

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Foreign Medical Graduate Research jobs near you
Infographic showing various Foreign Medical Graduate Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $91,466 per year, or $44 per hour.

Foreign Medical Graduate

DM Clinical Research

New York, NY • On-site

Full-time

Re-posted 4 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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