Senior Clinical Research Associate - 176687

Piper Companies; United States; Remote; USD 155.000 - 175.000; Vollzeit

Benefits dieser Stelle

Medical

Dental

Vision

401(k)

Paid leave

Zusammenfassung

Piper Companies seeks a Senior Clinical Research Associate to oversee oncology Phase II/III trials, often acting as the lead CRA on assigned studies. This 6-month remote contract with extensions targets candidates in the West or Central regions.

Responsibilities include managing site monitoring, serving as primary site liaison, ensuring protocol and regulatory compliance, and maintaining data quality with timely documentation.

Qualifikationen

• Minimum 2+ years of oncology monitoring experience with ~3 years of independent monitoring.
• Hands-on experience supporting Phase II/III oncology trials, ideally in a full-service model.
• Autonomous operator capable of serving as sole CRA with minimal oversight.

Aufgaben

• Independently manage site monitoring for Phase II/III oncology trials with mixed onsite/remote visits (8–10 onsite days/month).
• Serve as primary clinical contact for assigned sites and build long-term relationships.
• Ensure study conduct aligns with protocol, GCP and ICH guidelines.
• Oversee site performance, data quality, and risk mitigation.
• Prepare monitoring documentation including visit reports and follow-ups.

Kenntnisse

Oncology monitoring

Site management

Independent monitoring

Remote monitoring

Travel flexibility

Ausbildung

Bachelor’s degree not required

Tools

CTMS

EDC

Jobbeschreibung

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support oncology clinical trials for a well-established organization within the clinical research industry. This Senior Clinical Research Associate (CRA) role is a 6-month remote contract (with extensions), full-service position with a preference for candidates located in the West or Central regions. This individual will play a critical role overseeing Phase II and Phase III oncology studies, often functioning as the primary CRA on assigned trials.

Responsibilities of the Senior Clinical Research Associate include:

• Independently manage site monitoring activities for Phase II and III oncology trials, including a combination of onsite and remote visits averaging 8–10 onsite days per month.
• Serve as the primary clinical contact for assigned sites, building strong, long-term relationships and providing consistent support and guidance.
• Ensure study conduct aligns with protocol requirements, GCP, ICH guidelines, and applicable regulatory standards.
• Oversee site performance, data quality, and issue resolution while proactively identifying and mitigating risks.
• Prepare accurate and timely monitoring documentation, including visit reports and follow-up communications.

Qualifications for the Senior Clinical Research Associate include:

• Minimum of 2+ years of oncology monitoring experience with current expectations of approximately 3 years of independent monitoring.
• Hands‑on experience supporting Phase II and Phase III clinical trials, ideally within a full-service model working with biotechnology clients.
• Ability to operate autonomously, including serving as the sole CRA on a study and managing site relationships with minimal oversight.
• Willingness and ability to travel regionally, reside within one hour of a major airport, and maintain required onsite visit expectations.
• Bachelor’s degree not required for senior‑level consideration if equivalent clinical research experience can be demonstrated.

Compensation for the Senior Clinical Research Associate:

Salary: $155,000-$175,000/year (USD)

Benefits: Medical, Dental, Vision, 401(k), and applicable paid leave

This job opens for applications on 10/2/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: clinical research, clinical trials, CRA, oncology, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, patient recruitment, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk‑based monitoring, therapeutic areas.

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