Oncology Clinical Research Associate

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

Benefits offered by this job

Medical

Dental

Vision

401K

PTO

Holidays

Job summary

Piper Companies is seeking an experienced Oncology Clinical Research Associate (CRA) to join our client’s team. The Oncology CRA will monitor and manage trials, ensuring regulatory compliance and data integrity.

The role requires 3+ years of on-site CRA experience, willingness to travel 2–3 days per week, a valid driver’s license, and a life sciences-related degree. Compensation includes salary and comprehensive benefits.

Qualifications

• 3+ years of on-site CRA experience.
• Proficient with GCP guidelines and regulatory requirements.
• Strong organizational, time management, and communication skills.

Responsibilities

• Monitor trials to ensure adherence to protocols, GCP, and regulations.
• Perform site visits: pre-study, initiation, monitoring, and close-out.
• Review CRFs and source documents for accuracy and completeness.
• Report adverse events and protocol deviations promptly and accurately.

Skills

GCP compliance

Regulatory knowledge

Communication skills

Time management

Team collaboration

Independent worker

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 10/30/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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