International Medical Graduate (IMG) - Clinical Research Coordinator

About the role

Revival Research Institute, LLC is seeking an experienced Clinical Research Coordinator to join our dynamic team. Ideal candidates are detail-oriented, motivated learners with a strong interest in clinical research.

Responsibilities

• 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
• 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, research team and the Institutional Review Board
• Aid in 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

Requirements

• 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
• Radiology experience is preferred. Phlebotomy skills are also preferred.

Preferred 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

Pay

Competitive salary based on experience and qualifications.

Schedule

Full-time position with flexible working hours to accommodate clinical trial requirements.