Eupraxia Pharmaceuticals Inc.

Research Analyst

• 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

Clinical Research Associate

Clinical Research

• 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

Clinical Trial Manager

Marketing

• Lead the development of the 3-year strategic commercial plan.
• Analyze qualitative and quantitative market data.
• Develop and implement overarching marketing strategy (brand plan).
• Effectively communicate core branding, marketing messages and product positioning statements.
• Manage global brand marketing budget.
• Build relationships with Key Opinion Leaders (KOLs), patient advocacy groups, and customers.
• Oversee end-to-end launch planning, marketing, and promotional strategies for new and existing assets.
• Coordinate activities and resource planning of the global Market Access, Market Research, Patient Advocacy, and Medical groups.
• Establish the commercial analytics function.
• Monitor business results against stated objectives and initiate corrective actions.

Vice President, Marketing and Commercial Strategy

Paralegal

• Provide comprehensive legal and administrative assistance to the Legal, Compliance, and Privacy activities
• Draft, review, and maintain templates for contracts, NDAs, clinical trial agreements
• Manage the contract lifecycle using contract management systems
• Conduct legal research on pharmaceutical laws, data privacy, advertising, and anti-bribery regulations
• Support the implementation of compliance programs
• Prepare discovery materials, summarize documents, and coordinate with litigation counsel
• Support the Privacy Office with compliance under GDPR, HIPAA, CCPA
• Assist in managing data processing agreements and vendor due diligence