Clinical Research Coordinator (CRC)

We are seeking an experienced Clinical Research Coordinator (CRC) to join our team and support ongoing and future clinical trials in Los Angeles, CA. This role requires a highly independent professional who can manage various studies and adapt to site and study needs as required.

Responsibilities:

• Conduct and oversee clinical trial activities in compliance with study protocols.
• Ensure timely and accurate data entry into electronic databases.
• Obtain informed consent from research subjects.
• Perform vital sign assessments, blood draws, and other clinical procedures as needed.
• Monitor and document patient adverse events, collaborating with investigators and oversight agencies as necessary.
• Extract and analyze data from medical charts.
• Assist in quality assurance audits and monitoring visits by study sponsors/CROs.
• Prescreen potential candidates
• Maintain comprehensive study documentation, including case report forms, participant charts, and regulatory records.
• Perform additional duties as assigned.

Preferred Qualifications & Competencies:

• Spanish speaking preferred
• Minimum 2+ year of recent experience in clinical research.
• Clinical skills such as phlebotomy, ECG administration, and vital sign assessments are preferred but not mandatory.
• Strong ability to work independently and manage multiple studies.
• Willingness to commute to the study site as needed.
• Proficiency in EDC data entry and familiarity with EMR systems.

If you meet the qualifications and are interested in contributing to impactful clinical research, we encourage you to apply!

Pay: $20.00 - $35.00 per hour

Application Question(s):

• How many years have you been a CRC?

Work Location: In person