Sr. Contract Clinical Research Associate (Oncology)

Responsibilities

• Conduct site initiation, monitoring, and close-out visits for oncology studies.
• Ensure compliance with protocols, ICH-GCP, SOPs, and regulatory requirements.
• Verify source data, CRFs, and EDC entries for accuracy and completeness.
• Identify and document protocol deviations and safety issues.
• Prepare timely monitoring reports and maintain trial documentation.

Requirements

• 5+ years of CRA experience within pharmaceutical, biotechnology, or CRO settings.
• 3+ years of strong oncology clinical trial monitoring experience.
• Solid understanding of ICH-GCP and FDA regulations.
• Ability to independently manage multiple sites.
• Willingness to travel 8–10 days per month across PST, CST, and MST.

Compensation

$55.00 - $65.00 per hour (Depending on Experience)

Benefits

• Health
• Vision
• Dental
• Paid Time Off (PTO)
• Paid Holiday
• Paid Sick Leave (if required by law)

Keywords

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