Oncology Clinical Research Associate - 177216

Piper Companies; United States; Remote; USD 120,000 - 135,000; Full time

Benefits offered by this job

Salary range $120,000–$135,000

Comprehensive benefits

Job summary

Piper Companies is seeking an experienced Oncology Clinical Research Associate (CRA) to join our client’s team. This role focuses on monitoring trials, ensuring regulatory compliance, and maintaining data integrity and patient safety across oncology studies.

The CRA will conduct site visits, review CRFs, report adverse events, and provide training to site staff. Requires 3+ years on-site CRA experience, 70% travel, and a Bachelor’s degree in life sciences or related field.

Qualifications

• Minimum 3 years as on-site CRA.
• Willingness to travel up to 70% (2–3 days per week).
• Valid driver's license required.
• Familiarity with RECIST and CTCAE terminology.
• Solid understanding of clinical trial processes and regulatory requirements.
• Excellent organizational and time management skills.
• Strong written and oral communication abilities.
• Ability to work both independently and in a team.

Responsibilities

• Monitor trials for protocol adherence, regulatory compliance and GCP.
• Conduct site visits at pre-study, initiation, monitoring and close-out stages.
• Review CRFs and source documents for accuracy.
• Report adverse events and protocol deviations promptly.
• Train site staff on study procedures and regulatory requirements.
• Maintain communication with sites, investigators, and stakeholders.
• Assist with study documentation and monitoring plans.
• Participate in study team meetings and report site status.

Skills

On-site CRA experience

Travel readiness 70%

RECIST/CTCAE knowledge

Regulatory compliance knowledge

Strong communication

Teamwork & independence

Driver's license

Education

Bachelor's degree in life sciences, nursing, or pharmacy

Job description

Piper Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s team. This opportunity is with an industry-leading Oncology Clinical Research organization supporting one of the top pharmaceutical companies in the world. The Oncology CRA will play a critical role in monitoring and managing clinical trials, ensuring compliance with regulatory requirements, and maintaining high standards of data integrity and patient safety.

Responsibilities for the Oncology Clinical Research Associate:

• Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
• Review and verify case report forms (CRFs) and source documents for accuracy and completeness.
• Ensure timely and accurate reporting of adverse events and protocol deviations.
• Provide training and support to site staff on study protocols, procedures, and regulatory requirements.
• Maintain effective communication with study sites, investigators, and other stakeholders.
• Assist in the preparation and review of study-related documentation, including informed consent forms, study manuals, and monitoring plans.
• Participate in study team meetings and provide updates on site status and study progress.

Qualifications for the Oncology Clinical Research Associate:

• At least 3 years of experience as an On-site CRA.
• Comfortable with up to 70% travel (2-3 days per week).
• Must have a valid driver’s license.
• Must be comfortable handling questions regarding RECIST (Response Evaluation Criteria in Solid Tumors) and CTCAE (Common Terminology Criteria for Adverse Events).
• Strong understanding of clinical trial processes and regulatory requirements.
• Excellent organizational and time management skills.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Bachelor’s degree in a related field (e.g., life sciences, nursing, pharmacy).

Compensation/Benefits for the Oncology Clinical Research Associate:

• Salary: $120,000 - $135,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 10/26/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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