Clinical Research Coordinator — Impactful Trials & Compliance

Providence; Los Angeles (CA); Presencial; USD 46 000 - 71 000; Tempo integral

Resumo da oferta

Providence Caregivers in California is seeking a Clinical Research Coordinator to oversee the daily operations of multiple clinical studies under the Medical Office Administrator. You will coordinate with the Principal Investigator, patients, sponsors and the IRB to ensure smooth study progress.

The role emphasizes strict adherence to GCP/ICH, accurate documentation, and timely communication. A medical or phlebotomy training background and clinical research experience are preferred, with

Qualificações

• Accredited medical or phlebotomy training completed.
• College degree or vocational school graduation preferred.
• Phlebotomy certificate on hire for department SJuHMG Clinical Trials.
• 2–3 years of clinical research experience preferred.

Responsabilidades

• Oversee day-to-day functions of multiple clinical research studies.
• Interface with Principal Investigator, patients, sponsor, and the IRB.
• Ensure documentation is timely and accurate and that study protocols (GCP/ICH) are followed.
• Collaborate with the PI to ensure strict compliance with study protocols.

Formação académica

College degree

Vocational school graduation

Descrição da oferta de emprego

Providence Caregivers in California is seeking a Clinical Research Coordinator to oversee the daily operations of multiple clinical studies under the Medical Office Administrator. You will coordinate with the Principal Investigator, patients, sponsors and the IRB to ensure smooth study progress.

The role emphasizes strict adherence to GCP/ICH, accurate documentation, and timely communication. A medical or phlebotomy training background and clinical research experience are preferred, with