CRA - 173581

ZP Group; United States; Remote; USD 105,000 - 135,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k)

Travel reimbursement

Job summary

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support Phase II-III Oncology trials in a fast-paced biotech environment. Independent monitoring expertise and site partnership experience are highly valued, with hands-on trial execution across multiple oncology studies.

The role requires travel regionally, living within an hour of a major airport, and the ability to manage multiple sites with minimal oversight.

Qualifications

• Proven experience as a Senior CRA supporting oncology clinical trials.
• Strong background in independent monitoring, site management, and trial oversight.
• Deep understanding of ICH-GCP guidelines and clinical trial processes.
• Experience supporting Phase II-III oncology trials.
• Willingness to travel regionally; reside within one hour of a major airport.

Responsibilities

• Independently monitor Phase II-III oncology clinical trials in compliance with ICH-GCP, study protocols, and SOPs.
• Conduct on-site monitoring visits (8 days per month) including initiation, routine monitoring, and close-out.
• Perform SDR, SDV, and CRF review to ensure high-quality data.
• Build relationships with investigative sites to support enrollment and protocol adherence.
• Identify site-level risks and address issues to maintain timelines and quality.
• Collaborate with biotech sponsors, requiring strong communication and ownership.
• Manage multiple study sites and competing priorities with minimal oversight.

Skills

Senior CRA

Independent monitoring

Site management

ICH-GCP

Oncology trials

Client-facing

Travel readiness

Job description

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support Phase II-III Oncology clinical trials within a fast-paced biotechnology and clinical research environment. The Senior Clinical Research Associate (CRA) role is ideal for an experienced professional with strong independent monitoring expertise, site partnership experience, and a hands‑on approach to trial execution across multiple oncology studies.

Responsibilities of the Senior Clinical Research Associate (CRA):

• Independently monitor Phase II-III oncology clinical trials in compliance with ICH-GCP, study protocols, and SOPs.
• Conduct on‑site monitoring visits (approximately 8 days per month), including site initiation, routine monitoring, and close‑out visits.
• Perform source data review (SDR) and source data verification (SDV), as well as CRF review to ensure high‑quality, inspection‑ready data.
• Build strong relationships with investigative sites to support enrollment, protocol adherence, and overall study execution.
• Identify site‑level risks, proactively address issues, and elevate concerns to maintain timelines and quality standards.
• Collaborate directly with biotech sponsors, requiring strong communication, adaptability, and ownership of deliverables.
• Manage multiple study sites and competing priorities with minimal oversight in a high‑growth environment.

Qualifications of the Senior Clinical Research Associate (CRA):

• Proven experience as a Senior CRA supporting oncology clinical trials.
• Strong background in independent monitoring, site management, and trial oversight.
• Deep understanding of ICH-GCP guidelines and clinical trial processes.
• Experience supporting Phase II-III clinical trials within oncology.
• Ability to work directly with biotech clients in a fast‑paced, evolving environment.
• Strong organizational and problem‑solving skills with the ability to manage multiple priorities.
• Must reside within one hour of a major airport and be able to travel regionally to support assigned sites.

Compensation for the Senior Clinical Research Associate (CRA) includes:

• Salary range: $105,000 - $135,000
• Comprehensive benefits package including medical, dental, vision, and 401(k)
• Travel reimbursement and support for regional site monitoring
• Opportunity to work within a high‑growth, innovative clinical research environment

This job opens for applications on 09/2/2026. Applications for this job will be accepted for at least 30 days from the posting date.