Clinical Research Associate (CRA)

Zachary Piper Solutions is seeking a talented REMOTE Clinical Research Associate (CRA) to support a leading clinical research organization advancing innovative oncology studies. In this role, you will be responsible for ensuring study sites operate efficiently, maintain regulatory compliance, and successfully execute clinical trial protocols. You will work closely with investigators, site personnel, and study teams to support the delivery of high-quality clinical research and contribute to the advancement of groundbreaking oncology therapies.

Responsibilities of the Clinical Research Associate:

• Conduct site selection, initiation, monitoring, and close-out visits while ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Partner with study sites to develop, implement, and track recruitment plans to meet enrollment and project goals.
• Provide protocol training and maintain consistent communication with site personnel to manage expectations and resolve issues.
• Evaluate site practices for protocol adherence and identify, document, and escalate quality or compliance concerns as needed.
• Track regulatory submissions, patient recruitment, enrollment activities, data collection, and study progress to ensure milestones are achieved.
• Maintain Trial Master File (TMF) and Investigator Site File (ISF) documentation in accordance with regulatory and sponsor requirements.
• Support the development of clinical staff through co-monitoring activities, training visits, and mentorship.
• Collaborate with cross-functional study team members to support overall project execution and successful study outcomes.
• Manage site finances and assist with invoice retrieval and processing in accordance with local requirements.

Qualifications of the Clinical Research Associate:

• Bachelor's degree in a scientific discipline, healthcare, or a related field preferred.
• Minimum of three (3) years of on-site monitoring experience in oncology clinical trials.
• Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Experience supporting oncology protocols and clinical research studies.
• Proficiency with Microsoft Office applications.
• Excellent written and verbal communication skills.
• Strong organizational, problem-solving, and time-management abilities.
• Demonstrated ability to build and maintain strong working relationships with investigators, site personnel, and study teams.
• Effective financial management skills and experience managing site-related budgets and expenses.

Compensation of the Clinical Research Associate:

• $100,000-$130,000 salary based on experience, education, and qualifications.
• Comprehensive benefits package including Medical, Dental, Vision, 401(k), Paid Time Off, and additional company-sponsored benefits.

This job opens for applications on 07/13/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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