Clinical Research Associate

Eupraxia Pharmaceuticals Inc.

Clinical Research Associate responsible for managing clinical trial monitoring efficiently. Working at Eupraxia, a clinical-stage biotechnology company focused on innovative drug delivery solutions.

Posted 4/26/2026full-timeSeattle • Washington • 🇺🇸 United StatesJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Assisting Clinical Trial Manager in ensuring trials are initiated efficiently, completed on time, within budget and conducted in compliance with SOPs, regulations, and ICH/GCP guidelines
Assisting Clinical Trial Manager in managing CRO partners and other vendors
Working closely with and providing training to CRO staff, study site staff, and field-based CRAs
Overseeing, conducting, and/or co-monitoring site qualification, study initiation, interim monitoring, and close out visits and completing associated reports
Developing and/or assisting in the development of trial materials (e.g., protocol, informed consent forms, case report forms (CRF), CRF completion guidelines, monitoring guidelines, site initiation visit materials, site tools and worksheets, product administration guidelines)
Reviewing monitoring reports and monitoring visit letters written by CRO CRAs
Driving CRO and trial sites with study startup activities, including IRB/IEC submissions and ensuring collection and review of required essential documents
Creating, monitoring, and sharing key performance metrics with study teams
Reviewing completed CRFs and data listings for accuracy, overseeing data discrepancy management, and performing associated training/retraining to site staff and CRAs as needed
Developing strong and effective working relationships within Clinical Operations and other functional departments and CROs

Requirements

What you’ll need

BS/BA in life sciences or related discipline
5+ years pharma/biopharma industry experience, preferably in a sponsor-side role
1+ years of active, independent, on-site monitoring experience for all types of visits
Strong working knowledge of FDA and ICH/GCP regulations and guidelines
Thorough knowledge of clinical monitoring procedures
Strong interpersonal, communication (written and verbal), and organizational skills
Excellent analytical and assessment skills, judgment, and problem-solving skills

Benefits

Comp & perks

Must be willing to travel domestically and internationally (approximately 20-25%), as needed

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial managementsite qualificationstudy initiationinterim monitoringclose out visitsprotocol developmentcase report forms (CRF)data discrepancy managementmonitoring proceduresIRB/IEC submissions

Soft Skills

interpersonal skillscommunication skillsorganizational skillsanalytical skillsproblem-solving skillsjudgmenttraining skillsrelationship buildingcollaborationleadership