International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC•McKinney, TX

25d•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 Texas, Illinois, New Jersey, and North Carolina. We are recognized for our commitment to providing high-quality data for clinical research trials. As we continue to grow, we are seeking qualified professionals eager to develop their careers with us. This entry-level position is ideal for International Medical Graduates with a minimum of 3 years of research experience and a strong interest in Clinical Research, offering significant opportunities for advancement. While prior experience in clinical research is not mandatory, we are looking for detail-oriented, organized, and motivated individuals who are eager to learn and adapt to new therapeutic areas as our company expands.

Requirements

Minimum of 3 years of research experience.
Detail-oriented.
Ability to maintain organized records.
Motivated to learn new things.
Genuinely respectful of diverse points-of-view.
Ability to strive for an environment where 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.
Ability to 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.

Nice To Haves

International Medical Graduate (IMG).
Strong interest in the Clinical Research field.
Radiology experience.
Phlebotomy skills.
Knowledge of FDA Regulations and Good Clinical Practices.

Responsibilities

Coordinating and managing multiple studies.
Assisting Principal Investigators and other clinical staff with study-related tasks.
Research participant screening, recruitment, and enrollment.
Conducting research visits for data collection in no-risk or minimal-risk trials with oversight.
Collecting, processing, and shipping 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.