Clinical Research Coordinator - Los Angeles, United States - SQRL

Description

This role will be onsite in Northridge, CA

Responsibilities:

1. Study Coordination:

• Coordinate and oversee the planning and execution of clinical research studies per protocols and regulatory requirements.
• Work closely with principal investigators and other study team members to ensure the successful implementation of research projects.

1. Regulatory Compliance:

• Ensure adherence to regulatory standards and guidelines, including but not limited to FDA regulations, ICH/GCP guidelines, and institutional policies.
• Prepare and submit regulatory documents for study approval and maintain accurate and up-to-date regulatory files.

1. Participant Recruitment and Informed Consent:

• Recruit and screen eligible participants for clinical trials.
• Obtain informed consent from study participants and maintain proper documentation.

1. Data Collection and Management:

• Collect, record, and manage study data accurately and efficiently.
• Implement data quality control procedures and ensure data integrity throughout the study.

1. Communication and Collaboration:

• Serve as the primary point of contact for study participants and liaise with interdisciplinary team members, including physicians, nurses, and laboratory personnel.
• Communicate regularly with sponsors, monitors, and regulatory authorities as needed.

1. Training and Development:

• Provide training to research staff and ensure ongoing education on study protocols, procedures, and regulatory requirements.

Qualifications:

• Must have prior experience as a Clinical Research Coordinator in a healthcare or research setting (2+ years)
• Must have at least 1 year of experience in phlebotomy