Clinical Research Coordinator - Hybrid 6-Month Contract

Medix™; Long Beach (CA); Hybrid; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health benefits

Dental & Vision

401k

Paid sick leave

Life insurance

Disability insurance

Job summary

Medix is seeking a Clinical Research Coordinator in California to coordinate protocols from start-up to close-out while working with research staff to ensure data is collected, stored, and maintained in compliance with FDA, ICH and GCP.

The role involves source documents, data entry in EDC, regulatory submissions support, site feasibility, and coordination with sponsor/CRO. Hybrid work model with majority onsite; local candidates only.

Qualifications

• Coordinating clinical research protocols from start-up to close-out.
• Collect, store and maintain data in accordance with FDA, ICH and GCP.

Responsibilities

• Coordinate source documents, data collection and query resolution.
• Participate in data entry and reconciliation in EDC systems.
• Liaise with sponsor/CRO and research staff.
• Assist in regulatory submissions and IRB requirements.
• Support site feasibility, qualification visits and initiation visits.
• May recruit clinical trial participants.

Skills

Clinical coordination

Data entry

EDC systems

Regulatory submissions

Tools

EDC software

Job description

Medix is seeking a Clinical Research Coordinator in California to coordinate protocols from start-up to close-out while working with research staff to ensure data is collected, stored, and maintained in compliance with FDA, ICH and GCP.

The role involves source documents, data entry in EDC, regulatory submissions support, site feasibility, and coordination with sponsor/CRO. Hybrid work model with majority onsite; local candidates only.