Clinical Trial Manager
Eupraxia Pharmaceuticals Inc.
full-time
Posted on:
Location Type: Hybrid
Location: Seattle • Washington • United States
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Tech Stack
About the role
- Ensuring studies are carried out according to the study protocol, SOPs, and ICH/GCP guidelines/regulations
- Independently developing the trial’s timelines, budgets, key deliverables, and risk/mitigation strategies
- Leading the development of trial materials (e.g., protocol, informed consent forms, CRF)
- Planning and leading study team meetings
- Managing, mentoring, and training clinical operational staff
- Leading the identification and engagement of CROs and other third-party study vendors
Requirements
- Bachelor’s degree or equivalent in the life sciences
- At least 6 years of clinical operations experience in the pharmaceutical industry
- At least 1 year of experience managing industry sponsored pharmaceutical clinical trials as a sponsor employee
- Ability to plan, organize and conduct clinical trials with minimum oversight
- Experience leading, managing, or mentoring clinical operational staff and cross-functional teams
- Significant experience managing CROs and other vendors and assessing performance and finances
Benefits
- Health insurance
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical operationstrial managementbudget developmentrisk mitigation strategiesprotocol developmentinformed consent formsCRF developmentvendor managementperformance assessmentfinancial assessment
Soft Skills
leadershipmentoringtrainingplanningorganizationcommunicationteam managementindependencecollaborationproblem-solving
Certifications
Bachelor’s degree in life sciences