Clinical Research Coordinator, Immunology & Rheumatology

American Society of Gene & Cell Therapy; Cincinnati (OH); Híbrido; USD 65.000 - 85.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Comprehensive health coverage

Tuition remission

Retirement plans

Paid time off

Descripción de la vacante

University of Cincinnati College of Medicine seeks a Clinical Research Professional to support the Department of Internal Medicine, Division of Rheumatology, Allergy, and Immunology. The role spans the clinical research spectrum and collaborates with UC Health and Cincinnati Children's Hospital Medical Center to advance studies.

The position requires a Bachelor's degree in a related field and at least one year of related experience, with emphasis on regulatory compliance and IRB submissions.

Formación

• Bachelor’s Degree in a related field.
• Five years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements.

Responsabilidades

• Plan and coordinate clinical research projects.
• Screen patients for admission to study based on pre-determined criteria.
• Document and evaluate adverse events and response to treatment.
• Coordinate generation of data for proposals, reports, and manuscripts; assist in development of reports.
• Maintain regulatory documentation and prepare IRB submissions.
• Draft subject informed consents and consent comprehension tests.

Conocimientos

Clinical research coordination

Regulatory compliance

IRB submissions

Liaison with medical staff

Educación

Bachelor’s Degree in a related field

Descripción del empleo

University of Cincinnati College of Medicine seeks a Clinical Research Professional to support the Department of Internal Medicine, Division of Rheumatology, Allergy, and Immunology. The role spans the clinical research spectrum and collaborates with UC Health and Cincinnati Children's Hospital Medical Center to advance studies.

The position requires a Bachelor's degree in a related field and at least one year of related experience, with emphasis on regulatory compliance and IRB submissions.