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International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC·Elgin, Illinois

Full Time·On Site·2-5 yrs·Posted 3 months ago
Practice for this role

About the role

The Clinical Research Coordinator will manage multiple studies, including participant screening, recruitment, and enrollment. They are also responsible for collecting and processing research specimens, maintaining trial documentation, and assisting with regulatory document preparation.

[https://assets.jazz.co/customers/customer_20210831232649_IBKP8QMSBTZ6DVXB/layout/20220315184757-revival%20logo%20see%20through.png]

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, and Arizona. 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 Psych back ground. Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as 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!!!

Requirements

Candidates must be International Medical Graduates with at least 3 years of research experience and a background in psychology. Proficiency in Microsoft Office, strong organizational skills, and knowledge of FDA regulations and Good Clinical Practices are required.

  • postgraduate degree
  • Phlebotomy
  • Microsoft Office
  • Recruitment
  • Patient confidentiality
  • Quality control
  • Good Clinical Practices
  • Data collection
  • Specimen processing
  • Clinical research
  • Data integrity
  • FDA regulations
  • Participant screening
  • Case report forms
  • Electronic data capture
  • Regulatory document preparation

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Location
Elgin, Illinois
Posted
Apr 22, 2026
Closes
Jul 21, 2026
Application
Employer website
RR

Hiring organization

Revival Research Institute, LLC

Established in 2015, Revival Research Institute is devoted to researching causes and treatments for a variety of conditions, diseases, and ailments in multiple specialties. Learn more about our capabilities to provide you with the best service.

IndustryHospitals and Health Care
TypePrivately Held
Size201-500 employees
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Market context

Illinois physician roles remain competitive

Emergency Medicine physician roles in Illinois are typically driven by steady hospital and emergency department coverage needs, especially in larger metro and regional referral settings. These positions are competitive because employers usually expect active Illinois medical licensure, DEA certification, and board certification or eligibility, along with completed Emergency Medicine training. On this platform, job requirements and benefits are AI-summarized from the original job description, saving you research time; review the residency, licensure, and CME details closely before applying.

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