International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC•Southfield, MI

1d•Onsite

About The Position

Revival Research Institute, LLC, established in 2015 and headquartered in the Metro Detroit Region, has grown to have a national presence across multiple states. The institute is nationally acknowledged for its diligence in providing high-quality data for clinical research trials. As Revival Research Institute expands, it seeks qualified professionals to join its team and grow with the company. The position is for an International Medical Graduate with a minimum of 3 years of research experience, or an individual with a strong interest in the Clinical Research field for an entry-level role. The ideal candidate is detail-oriented, capable of maintaining organized records, and motivated to learn new things as the company expands into new therapeutic areas. New staff are expected to be genuinely respectful of diverse points-of-view and contribute to an inclusive environment that drives productivity and results.

Requirements

International Medical Graduate (IMG)
Minimum of 3 years of research experience (for IMGs)
Strong interest in the Clinical Research field (for entry-level positions)
Detail-oriented
Able to maintain organized records
Motivated to learn new things
Genuinely respectful of diverse points-of-view
Strive for an environment in which inclusiveness drives productivity and results
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
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

Nice To Haves

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
Document study related information in case report forms or electronic data capture systems
Handle data queries
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
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