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International Medical Graduate; IMG; Clinical Research Coordinator

Job in Hamilton Township, Mercer County, New Jersey, USA
Listing for: Revival Research Institute, LLC
Full Time position
Listed on 2026-09-12
Job specializations:
  • Research/Development
    Clinical Research, Medical Science
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below

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

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 3 years 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 include, but not limited to:

Responsibilities
  • 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
  • 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
  • Regulatory and quality. Maintain organization of all trial‑
  • 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
  • Professional and technical knowledge. Maintain professional and technical knowledge of clinical trials and standards of care
  • Participant confidentiality. Protect patient confidentiality
Preferred Qualifications
  • 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
  • Minimum of 3 years of research experience
  • Radiology experience is preferred. Phlebotomy skills are also preferred
  • 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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