Orthopedic Clinical Research Coordinator II

University of Arizona; Tucson (AZ); Presencial; USD 53.000 - 66.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Dental insurance

Vision insurance

Life insurance

Disability programs

Paid vacation

Sick leave

Holidays

Tuition reduction

Retirement plans

Descripción de la vacante

The University of Arizona seeks a Clinical Research Coordinator II in Orthopedic Surgery on the Tucson Campus. You will coordinate complex clinical studies under leadership and ensure compliance with protocols, regulatory requirements, and institutional policies.

Responsibilities include participant recruitment, informed consent, data collection, IRB submissions, regulatory management, study visits, and close-out activities, with collaboration with Principal Investigators and study sponsors.

Formación

• Bachelor's degree or equivalent required.
• Minimum of 3 years of relevant work experience.

Responsabilidades

• Coordinate study visits and procedures.
• Maintain regulatory and study documentation.
• Create source documents and training per study protocols and GCP.
• Perform participant pre-screening, recruitment, enrollment, and informed consent.
• Conduct study visits and clinical procedures per protocol.
• Maintain complete study documents and records.
• Develop study-specific tools and training materials.
• Manage regulatory documentation including IRB submissions and continuing reviews.
• Monitor adverse events and protocol deviations per requirements.
• Perform data collection, entry, and quality checks.
• Resolve data queries and maintain research databases.
• Coordinate all aspects of multiple trials with investigators.
• Handle biospecimen processing and storage per protocol.
• Maintain study supplies and equipment.

Educación

Bachelor's degree or equivalent advanced learning

Descripción del empleo

The University of Arizona seeks a Clinical Research Coordinator II in Orthopedic Surgery on the Tucson Campus. You will coordinate complex clinical studies under leadership and ensure compliance with protocols, regulatory requirements, and institutional policies.

Responsibilities include participant recruitment, informed consent, data collection, IRB submissions, regulatory management, study visits, and close-out activities, with collaboration with Principal Investigators and study sponsors.