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Clinical Research Associate (CRA)

ZP Group · zpgroup.com
United StatesRemoteMid level3+ yrs
Apply on ZP Group’s site

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Subscribers got this job on 23 October 2026. New jobs reach them at 8 am and 6 pm, 5 days before they open here. Get the next one first

The job in short

Clinical research associate monitoring.

GCPClinicalCompliance

Details

Found
6 d ago · posted 2026-10-23
Location as listed
REMOTE, Remote
Role
Lab / Clinical Research
Pay (as listed)
$155,000–$175,000 a year
Source
The company’s own careers site

Full 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 10/23/2026. Applications for this job will be accepted for at least 30 days from the posting date. #LI-JN1 #LI-REMOTE

Lab / Clinical Research jobs in the United States · All ZP Group jobs · Remote Lab / Clinical Research jobs in the United States

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