Senior CRA (Oncology) - 173726 - 174637

ZP Group; United States; Remote; USD 83,000 - 110,000; Full time

Benefits offered by this job

Travel reimbursement

Remote contract

Job summary

Piper Companies is seeking a Senior Clinical Research Associate (Oncology) to support a client in the biotechnology industry in the United States. This is a fully remote contract role with regional travel of approximately 25–40% to clinical trial sites.

The ideal candidate will bring a strong background in oncology trials, independent monitoring, and managing multiple sites with minimal oversight. The role involves performing site monitoring visits, ensuring GCP compliance, data quality, and

Qualifications

• 5+ years of CRA experience with at least 2+ years supporting oncology clinical trials.
• Strong experience with independent monitoring and full clinical trial lifecycle management.
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and oncology protocols.
• Experience working directly with biotech or sponsor clients in a fast-paced environment.
• Ability to manage multiple priorities effectively with approximately 25–40% travel.

Responsibilities

• Perform site monitoring visits across study phases, ensuring compliance with protocol, regulatory requirements, and GCP standards
• Maintain direct communication with investigative sites, providing guidance and resolving study-related challenges
• Oversee oncology study activities by reviewing data quality, patient safety measures, and overall site performance
• Manage multiple trial sites simultaneously, prioritizing deliverables and tracking key study milestones
• Collaborate with biotech sponsors and internal teams to support efficient and timely trial execution

Skills

CRA experience

Oncology trials

Independent monitoring

FDA regulations

ICH-GCP

Job description

Piper Companies is seeking a Senior Clinical Research Associate (Oncology) to support a client in the biotechnology industry in the United States. The Senior Clinical Research Associate (Oncology) role is a fully remote contract position with regional travel required to clinical trial sites. The Senior Clinical Research Associate (Oncology) role is ideal for an experienced professional with a strong background in oncology trials, independent monitoring, and managing multiple sites with minimal oversight.

Responsibilities of the Senior Clinical Research Associate (Oncology) include:

• Perform site monitoring visits across study phases, ensuring compliance with protocol, regulatory requirements, and GCP standards
• Maintain direct communication with investigative sites, providing guidance and resolving study‑related challenges
• Oversee oncology study activities by reviewing data quality, patient safety measures, and overall site performance
• Manage multiple trial sites simultaneously, prioritizing deliverables and tracking key study milestones
• Collaborate with biotech sponsors and internal teams to support efficient and timely trial execution

Requirements of the Senior Clinical Research Associate (Oncology) include:

• 5+ years of CRA experience with at least 2+ years supporting oncology clinical trials
• Strong experience with independent monitoring and full clinical trial lifecycle management
• In-depth knowledge of ICH‑GCP guidelines, FDA regulations, and oncology protocols
• Experience working directly with biotech or sponsor clients in a fast‑paced environment
• Ability to manage multiple priorities effectively with approximately 25–40% travel

Compensation for the Senior Clinical Research Associate (Oncology) include:

• $60 – $80/hour
• Contract role
• Travel reimbursement provided
• This job opens for applications on 9/25/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Senior Clinical Research Associate, CRA, Oncology, Clinical Trials, Remote, Contract, Monitoring, Biotech

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