More jobs:
Clinical Research Associate; CRA;
Remote / Online - Candidates ideally in
Indianapolis, Hamilton County, Indiana, 46262, USA
Listed on 2026-10-02
Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for:
Piper Companies
Remote/Work from Home
position Listed on 2026-10-02
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Job Description & How to Apply Below
Location: Indianapolis
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.
- 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.
- 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.
#LI-JN1
#LI-REMOTE
Position Requirements
10+ Years
work experience
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