International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC•Hamilton Township, NJ

9d•Onsite

About The Position

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. 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.

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 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.

Responsibilities

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.
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, e.g. study amendments, adverse event reporting, protocol deviation reporting.
Maintain professional and technical knowledge of clinical trials and standards of care.
Protect patient confidentiality.