Multisite Clinical Research Coordinator - Drive Phase I-IV Trials

alcanzaclinical; Gilbert (AZ); On-site; USD 42,000 - 66,000; Full time

Job summary

Alcanza is a growing clinical research organization with a network of sites across the United States. We are seeking a Clinical Research Coordinator (CRC) to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

The CRC will coordinate study activities, ensure data integrity, assist with site initiation and monitoring visits, manage documentation and communicate with investigators, sponsors, and participants in a compliant and patient-centric

Responsibilities

• Coordinate study activities to ensure timely and compliant execution of assigned protocols.
• Maintain data integrity and accurate documentation in accordance with GCP, ICH, HIPAA and FDA requirements.
• Assist with site initiation, monitoring visits, and regulatory submissions as needed.
• Communicate with investigators, sponsors, and study participants to ensure adherence to SOPs.

Job description

Alcanza is a growing clinical research organization with a network of sites across the United States. We are seeking a Clinical Research Coordinator (CRC) to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

The CRC will coordinate study activities, ensure data integrity, assist with site initiation and monitoring visits, manage documentation and communicate with investigators, sponsors, and participants in a compliant and patient-centric