Pediatric Clinical Research Coordinator II

Rady Children's Hospital-San Diego

Orange (CA)

In loco

USD 36.000 - 56.000

Tempo pieno

14 giorni+
Generatore di candidature

Una candidatura su misura per questa offerta di lavoro — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

Supera i filtri ATS

Descrizione del lavoro

CHOC Children’s in Orange, California seeks a Clinical Research Coordinator II to support multiple pediatric clinical studies under minimal supervision. You will manage feasibility, regulatory submissions to IRB, identify participants, coordinate data/specimens, and archive records per policy.

This mid-level role requires at least three years of experience, an associate degree (bachelor’s preferred), and knowledge of ICH-GCP and regulatory requirements. Cerner EMR experience is a plus.

Competenze

  • Minimum three years of clinical research coordination experience.
  • Basic knowledge of key regulatory requirements for human subjects and ICH-GCP.
  • Ability to conduct informed consent is preferred.

Mansioni

  • Coordinate and provide support to multiple human subjects (clinical) research projects.
  • Prepare materials for IRB submission and regulatory review.
  • Identify potential study participants and coordinate collection of data and specimens.
  • Maintain accurate study records and archival in accordance with policies.
  • Communicate across multiple teams and participate in quality assurance audits.
  • Ensure timely data collection and proper study materials management.

Conoscenze

Microsoft Office
Interpersonal skills
Communication
Detail oriented
Regulatory knowledge
ICH-GCP knowledge
Informed consent
Cerner EMR
Sample handling

Formazione

Associate degree
Bachelor’s degree

Strumenti

Cerner EMR

Descrizione del lavoro

CHOC Children’s in Orange, California seeks a Clinical Research Coordinator II to support multiple pediatric clinical studies under minimal supervision. You will manage feasibility, regulatory submissions to IRB, identify participants, coordinate data/specimens, and archive records per policy.

This mid-level role requires at least three years of experience, an associate degree (bachelor’s preferred), and knowledge of ICH-GCP and regulatory requirements. Cerner EMR experience is a plus.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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