Senior CRA / CRA II (Oncology)

Piper Companies; Portland (OR); On-site; USD 110,000 - 120,000; Full time

Job summary

An established industry player is seeking a motivated Clinical Research Associate with Oncology Clinical Trials experience. This role involves developing relationships with investigative sites, monitoring clinical trial data accuracy, and ensuring compliance with regulatory standards. The ideal candidate will have over two years of clinical monitoring experience and a strong background in Oncology. Join a dedicated team focused on improving the drug development process while enjoying comprehensive benefits and a competitive salary range. If you are passionate about clinical research and want to make a difference, this opportunity is perfect for you.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401k

Paid Time Off

Sick Leave

Holidays

Qualifications

• 2+ years of clinical monitoring experience required; CRO preferred.
• Experience with FDA, ICH GCP, and local regulations.

Responsibilities

• Develop and maintain relationships with investigative sites and client personnel.
• Monitor sites for accuracy and validity of entries related to patient records.

Skills

Clinical Monitoring

Oncology Experience

Communication Skills

Interpersonal Skills

Organizational Skills

Job description

Piper Companies is currently seeking a motivated Clinical Research Associate with Oncology Clinical Trials experience to work for a well-established clinical research organization and pharmaceutical company focused on improving the drug development process. Candidates for this opportunity must be located in Oregon (or another PST state).

Responsibilities of the Senior Clinical Research Associate / CRA II:

• Develop and maintain relationships with investigative sites and client personnel.
• Monitor sites for accuracy and validity of entries related to patient records and clinical notes.
• Provide and communicate trial status and progress reports to trial manager and client.
• Manage and maintain the data and documents required by local and ICH regulatory authorities.
• Ensure SOPs are being followed and assist with client audits and regulatory inspections.

Qualifications of the Senior Clinical Research Associate / CRA II:

• 2+ years of clinical monitoring experience required; CRO preferred.
• 1+ years of experience within the therapeutic area of Oncology.
• Experience with FDA, ICH GCP, and local regulations.
• Strong communication, interpersonal, and organizational skills necessary.

Compensation for the Senior Clinical Research Associate / CRA II:

• Salary Range: $110,000-$120,000 based on experience.
• Comprehensive Benefits including Medical, Dental, Vision, 401k, PTO, Sick Leave if required by law, & Holidays.

This job opens for applications on 3/18/2025. Applications for this job will be accepted for at least 30 days from the posting date.