Senior Clinical Research Coordinator: Impactful Trials

Profound Research; South Gate (CA); Sur place; USD 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Full benefits package

Résumé du poste

Profound Research is seeking a Senior Clinical Research Coordinator to ensure site compliance and coordinate all activities for multiple clinical trials on-site. The role requires strong knowledge of FDA regulations, ICH-GCP, and trial protocols, with the ability to train teammates and lead regulatory and data collection tasks.

The candidate should have a Life Sciences degree or equivalent, multiple years of CRC experience, and certification such as GCP/CCRC.

Qualifications

• BS/BA in Life Sciences or related field required; 4+ years as a CRC.
• Associate degree with 6+ years as CRC or High School with 8+ years as CRC.
• GCP certification required; CCRC certification preferred.

Responsabilités

• Maintain site compliance for clinical trial activities per protocols, laws, and SOPs.
• Maintain knowledge of FDA regulations, ICH-GCP, SOPs, and study protocols.
• Complete required Profound Research training including ICH-GCP and IATA.

Connaissances

BS/BA Life Sciences

Clinical Research Coordinator

GCP certification

CCRC certification

Attention to detail

Communication skills

Formation

BS/BA in Life Sciences

Associate degree

High School/GED

Description du poste

Profound Research is seeking a Senior Clinical Research Coordinator to ensure site compliance and coordinate all activities for multiple clinical trials on-site. The role requires strong knowledge of FDA regulations, ICH-GCP, and trial protocols, with the ability to train teammates and lead regulatory and data collection tasks.

The candidate should have a Life Sciences degree or equivalent, multiple years of CRC experience, and certification such as GCP/CCRC.