Pediatric Clinical Research Coordinator — Onsite

Cincinnati Children's; Cincinnati (OH); Presencial; USD 57.000 - 62.000; Jornada completa

Descripción de la vacante

Cincinnati Children's is seeking Clinical Research Coordinators to support innovative clinical and translational research programs across multiple specialties. CRCs may coordinate participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process specimens, oversee study data, and ensure compliance with research protocols and regulatory requirements.

Please note, this onsite position is located in Cincinnati, Ohio, and offers opportunities to work

Formación

• Bachelor's degree in a scientific/health field and ≥1 year of related work experience, or a Master's degree.
• Strong organizational, communication, and problem-solving skills.
• Ability to manage multiple priorities with attention to detail.
• Proficiency with Microsoft Office applications.

Responsabilidades

• Coordinating day-to-day research study activities
• Recruiting, screening, consenting, and retaining study participants
• Scheduling and conducting study visits
• Maintaining research records and source documentation
• Managing regulatory submissions and study approvals
• Entering and validating study data in electronic databases
• Collecting, processing, and shipping research specimens
• Collaborating with investigators, sponsors, clinical teams, and research participants
• Supporting study monitoring visits, audits, and quality assurance activities
• Ensuring compliance with protocols, institutional policies, Good Clinical Practice (GCP), and regulatory requirements

Conocimientos

Organizational skills

Communication skills

Problem solving

Educación

Bachelor's or Master's in a science/health field

Herramientas

Microsoft Office

Descripción del empleo

Cincinnati Children's is seeking Clinical Research Coordinators to support innovative clinical and translational research programs across multiple specialties. CRCs may coordinate participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process specimens, oversee study data, and ensure compliance with research protocols and regulatory requirements.

Please note, this onsite position is located in Cincinnati, Ohio, and offers opportunities to work