Full-time
Clinical Research Associate-Freelance
Competitive
Full-time, ContractScience & PharmaceuticalPosted 26d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
26 days ago
Job description
TRIO (Translational Research in Oncology) is a global academic clinical research organization dedicated to advancing translational cancer research through clinical trials. The organization is seeking a Clinical Research Associate or Senior Clinical Research Associate to perform clinical trial monitoring activities, ensure regulatory and ICH-GCP compliance, support data validation, and collect required documentation.
Tags
Health Care
Life Science
Biotechnology
Healthcare
Oncology
2 email credits available today
Beyond your network
Vice President Human Resources
From your previous company
& 2 connections
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from your School
Responsibilities
Performing data verification of source documents
Conducting site visits, including pre-study, initiation, monitoring, and termination
Confirming adherence to all FDA, ICH-GCP, and local regulations
Ensuring implementation and compliance with FDA, and ICH-GCP guidelines
Assisting with data validation and query resolution
Mentoring junior team members as required
Ensuring the completion and collection of regulatory documents
Preferred
Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred
Benefits
Remote work arrangement
One-year contract
Full-time availability
TRIO is an academic clinical research organization that is dedicated to advancing translational cancer research.
Edmonton, Alberta, CAN
http://www.trioncology.org
Growth Stage
Leadership Team
Alexandra Neff
Chief Financial Officer
Recent News
PharmiWeb
Onco-Innovations Appoints Dr. John Mackey to Scientific & Clinical Advisory Board
2025-09-12
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Qualifications
A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse
Minimum of 1 year monitoring experience on an early phase trial
Fluent in English
Completion of a science-related Bachelor's degree
Excellent knowledge of medical terminology and clinical monitoring process
Strong ICH-GCPs knowledge
Experience with clinical trial information systems
Must be legally authorized to work in the United States
Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred
A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse;
Required skills
Oncology Clinical Research, Clinical Trial Monitoring, Early-Phase Clinical Trials, Phase I Clinical Trials, Solid Tumor Trials, ICH-GCP, FDA Regulations, Medical Terminology, Clinical Trial Information Systems
Experience
3+ years
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