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Revival Research Institute, LLC

Clinical Research Coordinator Womens health

Revival Research Institute, LLC, Dearborn Heights, Michigan, United States, 48127

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Unique opportunity to make an impact in the healthcare industry… Revival Research Institute, LLC

was established in 2015 and headquartered in the Metro Detroit Region. We have been growing steadily and now have a national presence in the

Metro-Detroit Region, Texas, Illinois, Georgia, and North Carolina.

We are nationally recognized for our commitment to providing high-quality data for clinical research trials. As

Revival Research Institute

continues to grow, we are looking to add qualified professionals to our team who are eager to grow and learn with us. We are seeking a full-time

Clinical Research Coordinator

with a minimum of 2 years of clinical experience for our Women's Health site. An individual with a strong interest in clinical research would be an excellent fit for this entry-level position with room to grow. However, this background is not mandatory, as our ideal candidate is detail-oriented, organized, motivated to learn, and eager to grow with our expanding company into new therapeutic areas. Clinical Research Coordinators at

Revival Research Institute

should respect diverse viewpoints and strive for an inclusive environment that fosters productivity and results. They are responsible for coordinating and managing multiple studies, assisting investigators and clinical staff with study-related tasks, including but not limited to: Participating in participant screening, recruitment, and enrollment; conducting research visits for data collection, minimal risk trials, or no study article trials; responsible for collecting, processing, and shipping specimens where applicable. Documenting study-related information in case report forms or electronic data systems; handling data queries and participating in monitoring visits; maintaining source documents. Organizing all trial-related documents and correspondence; implementing quality control and assurance measures. Communicating with study sponsors, research teams, and the Institutional Review Board; assisting with regulatory document preparation, study amendments, adverse event reporting, and protocol deviations. Maintaining professional and technical knowledge of clinical trials. Communicating with research participants and their families, ensuring patient confidentiality. Preferred Qualifications: Education/Training: Bachelor's degree in a health-related field with 1-2 years of relevant clinical experience, or a Master's degree in a medical-related field. Candidates with more experience may be considered for higher positions. Phlebotomy skills are preferred. Certifications: National Certification (CRA or ACRP), BLS Certification. Additional Skills: Proficiency in database management and computer skills (Microsoft Office suite), excellent verbal and written communication, ability to work independently, strong organizational skills, and ability to meet deadlines while maintaining confidentiality. Knowledge of FDA regulations and Good Clinical Practices is preferred. IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!

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