Live opening · Posted 9 days ago

Clinical Research Associate (CRA) - 174335

CHEManager International · United States (Remote)
Linkedin No
You are 9 days behind. JobBeeper subscribers saw this role while it was still new.

At a glance

The key details from the original listing.

Posted 9 days ago
CompanyCHEManager International
LocationUnited States (Remote)
Salary401(k) benefit
Work modeNo
SourceLinkedin
Listed9 days ago

Your early-applicant advantage

Live timing from JobBeeper.

Live data
27 min from Linkedin publishing this role to us finding it
9 min median time from a role going live to a subscriber being told
6 hours subscribers had this role before this page existed
70,984 roles found in the last 24 hours — the newest are not on this site yet
Start your free trial →

About the role

Description supplied by the original job listing.

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 9/14/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Work arrangement
No

Get JobBeeper Mobile App

Never miss a job opening! Get instant job alerts on your phone.

Subscribers see fresh openings within minutes. Download the JobBeeper App on Google Play to get real-time push notifications and apply before anyone else.

⚡ Instant Push Alerts 🎯 Tailored Filters 🚀 Direct Employer Links
GET IT ON Google Play

More openings worth a look

Recently tracked roles with full details and direct application links.

6 roles
Good roles move before most people even see them. Tell JobBeeper what you want and get fresh matches delivered in minutes.
Start your free trial →
⚡ Get fresh job alerts 📱 Get App