Oncology CRA

Piper Companies; United States; On-site; USD 120,000 - 130,000; Full time

Benefits offered by this job

Health, Vision, Dental

Paid Time Off & Holidays

Job summary

Piper Companies is actively seeking an Oncology CRA for a fully remote role with travel within the United States. The CRA will oversee site activities to ensure compliant, high-quality conduct across global clinical programs.

Responsibilities include site monitoring, training delivery, site recruitment collaboration, and tracking milestones. The role requires Oncology on-site monitoring experience, strong regulatory knowledge, and excellent communication and project-management skills.

Qualifications

• Bachelor’s degree in life sciences, healthcare, or related field.
• Minimum 3 years of on-site Oncology monitoring experience, including Phase I studies.
• Strong knowledge of GCP/ICH guidelines and oncology trial protocols.
• Proven ability to manage sites, monitor conduct, and ensure data quality and patient safety.
• Excellent communication, organizational and time-management skills.

Responsibilities

• Perform site selection, initiation, monitoring, and close-out visits.
• Collaborate with sites to drive patient recruitment and enrollment.
• Deliver protocol and study-specific training and address operational issues.
• Monitor protocol adherence, identify quality concerns, and escalate regulatory issues.
• Track milestones like regulatory submissions, site activation, patient recruitment, and data management.
• Maintain trial documentation (TMF/ISF) and support site budgeting and invoicing; mentor staff.

Skills

GCP/ICH knowledge

On-site monitoring

Regulatory compliance

Communication & stakeholder management

Education

Bachelor’s degree in life sciences or related field

Tools

MS Office

Job description

Piper Companies is actively seeking an Oncology CRA to join a CRO supporting global clinical program. The Oncology CRA will be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.

The Oncology CRA role is a fully remote position with travel (U.S.-based).

Responsibilities of the Oncology CRA:

• Conduct site selection, initiation, monitoring, and close-out visits to ensure compliance with GCP, ICH, protocol requirements, and applicable regulatory standards.
• Partner with investigative sites to develop, track, and execute patient recruitment and enrollment strategies to meet study objectives and timelines.
• Deliver protocol and study-specific training, maintain ongoing communication with site personnel, and proactively address operational issues and risks.
• Monitor study conduct and site performance, assess protocol adherence, identify quality concerns, and elevate issues to support regulatory compliance and data integrity.
• Track study milestones including regulatory submissions, site activation, patient recruitment, enrollment, and data management activities to ensure successful study execution.
• Maintain essential trial documentation within TMF and ISF files, support site financial management and invoice processing, and mentor clinical staff through training, co-monitoring, and collaborative study support.

Qualifications of the Oncology CRA:

• Bachelor’s degree in a scientific, life sciences, healthcare, or related discipline preferred.
• Minimum of 3 years of recent on-site clinical monitoring experience in Oncology, with direct experience supporting Phase I studies involving solid and/or liquid tumor indications; this requirement is mandatory.
• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, regulatory requirements, and oncology clinical trial protocols.
• Proven ability to independently manage investigative sites, monitor study conduct, ensure protocol compliance, and maintain high standards of data quality and patient safety.
• Proficiency with Microsoft Office applications, along with excellent communication, organizational, problem-solving, and relationship-management skills.
• Demonstrated ability to effectively manage timelines, budgets, and competing priorities while building strong collaborative partnerships with investigators, site personnel, and cross-functional study teams.

Compensation for the Oncology CRA:

• Salary Range: $120,000 – $130,000, depending on experience
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

This job opens for applications on 7/29/26. Applications will be accepted for at least 30 days from the posting date.

Keywords:

Clinical Research Associate, CRA, Clinical Trials, Monitoring, Remote, Site Monitoring, Data Review, Regulatory, Life Sciences, Biotech, Pharmaceutical, Study Management, Patient Safety

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