CRA - 173581 - 177428

Piper Companies; United States; À distance; USD 105 000 - 135 000; Plein temps

Avantages offerts par ce poste

Medical benefits

Dental benefits

Vision benefits

401(k)

Résumé du poste

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support Phase II–III oncology trials within a fast-paced biotechnology setting. The Senior CRA brings hands-on trial execution, independent monitoring expertise, and strong site partnerships to ensure data quality and study progress.

The role requires travel to regional sites, close collaboration with sponsors, and strict adherence to ICH-GCP guidelines across multiple studies.

Qualifications

• Senior CRA with oncology trial experience.
• Strong independent monitoring and site management expertise.
• Willingness to travel regionally; reside near a major airport.

Responsabilités

• Independently monitor Phase II–III oncology trials in line with ICH-GCP, protocols and SOPs.
• Conduct on-site monitoring visits roughly 8 days per month including initiation, routine monitoring and close-out.
• Perform SDR/SDV and CRF reviews to ensure high-quality, inspection-ready data.
• Build strong relationships with investigative sites to support enrollment and protocol adherence.
• Identify site risks, proactively address issues and elevate concerns to maintain timelines and quality.
• Collaborate with biotech sponsors; demonstrate clear communication and ownership of deliverables.
• Manage multiple study sites and priorities with minimal oversight in a fast-growing environment.

Connaissances

Independent monitoring

Site management

Trial oversight

ICH-GCP

Oncology trials

Description du poste

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 10/29/2026. Applications for this job will be accepted for at least 30 days from the posting date.