International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC•Elgin, IL

1d•Onsite

About The Position

Revival Research Institute, LLC, established in 2015 and headquartered in the Metro Detroit Region, has expanded its national presence to include Metro-Detroit, Texas, Illinois, and Arizona. The institute is recognized for its commitment to providing high-quality data for clinical research trials. As Revival Research Institute continues to grow, it seeks qualified professionals to join its team and develop their careers. This entry-level position offers opportunities for growth and is ideal for International Medical Graduates with a minimum of 3 years of research experience and a background in psychology. Candidates with a strong interest in the Clinical Research field are also encouraged to apply, even if they lack a psychology background, as the company values detail-orientation, organizational skills, and a motivation to learn new things, especially as it expands into new therapeutic areas. New team members are expected to be respectful of diverse viewpoints and contribute to an inclusive and productive work environment.

Requirements

International Medical Graduate (IMG)
Minimum of 3 years of research experience
Psych background (preferred, but not strictly necessary if strong interest in Clinical Research and other qualities are present)
Detail-oriented
Ability to maintain organized records
Motivated to learn new things
Genuinely respectful of diverse points-of-view
Ability to work independently and assume responsibility
Excellent organizational skills
Ability to meet data deadlines
Ability to maintain confidentiality
Ability to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff
Knowledge of FDA Regulations and Good Clinical Practices
Database and computer skills: Microsoft Office (Word, Excel), Outlook
Excellent verbal and written communication skills

Nice To Haves

Strong interest in the Clinical Research field
Radiology experience
Phlebotomy skills

Responsibilities

Coordinating and managing multiple studies
Assisting the Principal Investigators and other clinical staff with study related tasks
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
Collecting, processing and shipping of research specimens, where applicable
Documenting study related information in case report forms or electronic data capture systems
Handling data queries and participating in monitoring visits
Obtaining, reviewing and maintaining source documents
Maintaining organization of all trial related documents and correspondence
Implementing quality control and assurance methods
Communicating with study sponsors, research team and the Institutional Review Board
Assisting with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting
Maintaining professional and technical knowledge of Clinical trials and Standards of Care
Protecting patient confidentiality
Maintain data integrity within the department