Clinical Research Associate: Site Monitoring & Data Integrity

Comunidade Metodista; Los Angeles (CA); On-site; USD 85,000 - 110,000; Full time

Job summary

RDI is seeking a detail-oriented Clinical Research Associate to monitor trials, ensure protocol and regulatory compliance, and support site staff across multiple sites. The role emphasizes data integrity, patient safety, and collaboration with investigators in a fast-paced research environment.

Ideal candidates will have a life sciences background, 2+ years of CRA experience, strong GCP knowledge, and excellent communication skills.

Qualifications

• Bachelor's degree in life sciences, nursing, or related field; advanced degree preferred.
• Minimum 2 years of CRA or similar clinical research experience.
• Strong knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Excellent communication and interpersonal skills.
• Ability to travel to various clinical sites as required by the study protocol.

Responsibilities

• Conduct site visits including initiation, monitoring, and closeout activities to ensure protocol compliance.
• Collaborate with investigators and site staff to train on study procedures.
• Review and verify clinical data for accuracy and completeness per GCP.
• Prepare progress reports and keep stakeholders informed about study status.
• Identify and resolve site issues, discrepancies, and non-compliance to protect study integrity.
• Assist in the selection and evaluation of study sites.
• Manage study supplies and ensure timely delivery to clinical sites.

Skills

Good Clinical Practice

Education

Bachelor's degree in life sciences or related field

Advanced degree preferred

Tools

CTMS

Job description

RDI is seeking a detail-oriented Clinical Research Associate to monitor trials, ensure protocol and regulatory compliance, and support site staff across multiple sites. The role emphasizes data integrity, patient safety, and collaboration with investigators in a fast-paced research environment.

Ideal candidates will have a life sciences background, 2+ years of CRA experience, strong GCP knowledge, and excellent communication skills.