Clinical Research Associate - Site Monitoring & Trials

IQVIA; California; On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking an on-site Clinical Research Associate (CRA) to monitor study sites, ensure protocol adherence, and support regulatory submissions. You will manage site visits, train site staff, and collaborate with the project team to meet study milestones.

The role requires 2+ years of CRA experience, strong knowledge of GCP/ICH, and proficiency in MS Office within a fast-paced CRO or sponsor environment. Based in California, US.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Requires at least 2 years of on-site monitoring experience as a Clinical Research Associate (CRA).
• Good knowledge of GCP and ICH guidelines.
• Proficiency in MS Word, Excel and PowerPoint; laptop/phone usage.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) per scope and GCP.
• Drive subject recruitment plan with sites to enhance predictability.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol compliance and regulatory adherence.
• Track regulatory submissions, recruitment, CRF completion, data queries and resolutions.

Job description

IQVIA is seeking an on-site Clinical Research Associate (CRA) to monitor study sites, ensure protocol adherence, and support regulatory submissions. You will manage site visits, train site staff, and collaborate with the project team to meet study milestones.

The role requires 2+ years of CRA experience, strong knowledge of GCP/ICH, and proficiency in MS Office within a fast-paced CRO or sponsor environment. Based in California, US.