Oncology Clinical Research Associate - 175752

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

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401K

Paid Time Off

Holidays

Job summary

Piper Companies seeks an experienced Oncology Clinical Research Associate to monitor trials and ensure data integrity and patient safety across sites in the United States. This role emphasizes regulatory compliance and high-quality monitoring practices.

The position requires 3+ years of on-site CRA experience, up to 70% travel (2–3 days per week), a valid driver’s license, and a life sciences-related bachelor’s degree. Competitive salary and comprehensive benefits are offered.

Qualifications

• 3+ years of on-site CRA experience.
• Willing to travel up to 70% (2–3 days per week).
• Must have a valid driver’s license.
• Must be comfortable handling RECIST and CTCAE questions.
• Strong understanding of clinical trial processes and regulatory requirements.

Responsibilities

• Monitor trials to ensure protocol, regulatory, and GCP compliance.
• Conduct pre-study, initiation, monitoring, and close-out visits.

Skills

On-site CRA experience

70% travel

Driver's license

RECIST/CTCAE knowledge

Regulatory compliance

Organizational skills

Communication skills

Team collaboration

Education

Bachelor’s degree in life sciences / nursing / 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 10/2/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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