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Job Description
Arizona Liver Health is seeking a TEMPORARY Clinical Research Coordinator III to manage clinical research activities in compliance with FDA CFR, GCP, and company SOPs. The Clinical Research Coordinator III will be responsible for coordinating and implementing assigned protocols under the direction of the Principal Investigator or sub-investigator. This role involves collecting and recording clinical research data, assisting in patient assessments, scheduling, and maintaining study files, supplies, and medication accountability.
Role involves:
- Managing the conduct of clinical research activities.
- Coordinating and implementing assigned protocols.
- Collecting and recording clinical research data.
- Assisting in patient assessments and scheduling.
- Maintaining study files, supplies, and medication accountability.
- Recruiting and screening potential participants.
- Ensuring adherence to protocol requirements.
- Overseeing specimen collection, storage, and shipment.
Requirements:
- Minimum of four (4) years of experience working previously in a clinical research coordinator role.
- Experience and training in the conduct of clinical research.
- Thorough understanding of regulatory requirements, principles of GCP, and biomedical research ethics.
- Interpersonal and communication skills.
- Knowledge of all active protocols and disease indications within the company.
- Associates or Bachelor's degree in healthcare, clinical research management, or related field required.
- GCP certification required at hire.
Role offers:
- Compensation: $40-$45 per hour, depending on experience
- Status: Full-time, 3-Month Contract (eligible for overtime)
- Work Schedule: Monday-Friday, 7am-4pm (set schedule)
- 5 days Sick Time
- Shared company vehicles for required travel
