International Medical Graduate (IMG) - Clinical Research

Revival Research Institute, LLC•Southfield, MI

10d•Onsite

About The Position

Revival Research Institute is seeking International Medical Graduates with at least one year of research experience to join their team. The role involves coordinating research visits and maintaining study documentation under supervision. Clinical Research Coordinators are responsible for managing multiple studies and supporting Principal Investigators and other clinical staff with various study-related tasks.

Requirements

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 1 year 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.

Responsibilities

Screen, recruit, and enroll research participants.
Obtain consent and conduct research visits for data collection for no-risk or minimal-risk trials with oversight.
Collect, process, and ship research specimens, where applicable.
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.
Maintain organization of all trial-related documents and correspondence.
Implement quality control and assurance methods.
Communicate with study sponsors, the research team, and the Institutional Review Board.
Assist with basic regulatory document preparation with oversight, such as study amendments, adverse event reporting, and protocol deviation reporting.
Maintain professional and technical knowledge of clinical trials and standards of care.
Protect patient confidentiality.