CRA - 173581

Piper Companies

United States

Remote

USD 105,000 - 135,000

Full time

14 days+

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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k)

Job summary

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support Phase II-III Oncology trials within a fast-paced biotechnology and clinical research environment. The role emphasizes independent monitoring, site partnerships, and hands-on trial execution across multiple oncology studies.

The Senior CRA will monitor trials, perform SDR/SDV, ensure quality data, and travel regionally, residing within one hour of a major airport. Strong ICH-GCP knowledge is required.

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.
  • 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.

Responsibilities

  • 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.

Skills

Independent monitoring
Site management
Trial oversight
ICH-GCP knowledge
Oncology trials
Regional travel

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.

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