Clinical Research Associate (CRA)

Zp Group Llc

  • NY
  • 30+ days ago
  • Remote
  • $155,000–$175,000 Per Year

Highlights

The Clinical Research Associate (CRA) role is ideal for an experienced monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol compliance across multi-site trials. Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry.

Numbers & Facts

LocationNY (
Remote
)
Salary$155,000–$175,000 Per Year

Description

Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol compliance across multi-site trials. This role is fully remote for candidates with occasional travel required.

Responsibilities of the Clinical Research Associate:

  • Oversee and manage oncology clinical trial sites to ensure protocol compliance, data integrity, patient safety, and adherence to GCP, and SOPs.
  • Conduct site qualification, initiation, interim monitoring, and close-out visits for oncology clinical trials.
  • Ensure clinical trial activities are conducted in compliance with ICH-GCP, FDA regulations, and study protocols.
  • Review and verify source data, case report forms (CRFs), and regulatory documentation for accuracy and completeness.
  • Identify, document, and follow up on site issues, protocol deviations, and corrective action plans.
  • Serve as the primary point of contact for investigative sites, providing ongoing training and support.
  • Collaborate with cross-functional teams including Clinical Operations, Data Management, and Project Management.
  • Prepare detailed monitoring visit reports and maintain accurate trial documentation.

Qualifications of the Clinical Research Associate:

  • 3+ years of experience as a Clinical Research Associate monitoring interventional clinical trials.
  • Hands‑on experience performing onsite monitoring for oncology studies, ensuring GCP compliance and inspection readiness.
  • Direct oncology trial monitoring experience is required.
  • Strong knowledge of ICH-GCP guidelines, FDA regulations, and clinical research best practices.
  • Experience conducting remote and on-site monitoring visits independently.
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to travel occasionally to investigative sites as required.

Compensation for the Clinical Research Associate includes:

  • Salary range: $155,000 - $175,000 depending on experience
  • Comprehensive benefits package including medical, dental, vision, 401(k), and PTO
  • Fully remote work environment with occasional travel

This job opens for applications on 7/17/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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