Remote Clinical Trials Project Manager at Elpida
Remote / Online - Candidates ideally in
Lévis, Québec, Province de Québec, Canada
Listed on 2026-07-07
Lévis, Québec, Province de Québec, Canada
Listing for:
Elpida Therapeutics
Remote/Work from Home
position Listed on 2026-07-07
Job specializations:
-
Research/Development
Clinical Research, Regulatory Compliance Specialist
Job Description & How to Apply Below
Lead global clinical trials from Canada as a Clinical Trials Project Manager with Elpida Therapeutics. This remote position focuses on driving project success while ensuring compliance and engagement across multiple rare disease initiatives.
Elpida Therapeutics seeks a skilled Clinical Trials Project Manager to manage the execution of international trials. You will oversee all aspects, including project plans, timelines, and budgets.
Your role includes working with investigators, hospitals, and regulatory bodies to advance critical therapies for children with ultra-rare diseases.
Key Responsibilities:
• Manage day-to-day clinical trial operations internationally
• Develop and maintain project timelines and budgets
• Coordinate site activities and regulatory submissions
• Lead patient enrollment and engagement strategies
• Ensure compliance with ethical and regulatory guidelines
Requirements:
• Minimum 5 years in clinical trial management
• Solid knowledge of ICH-GCP regulations
• Experience with CROs and healthcare professionals
• Excellent communication skills and multitasking ability
• Authorized to work in Canada
Drive significant outcomes in the field of pediatric medicine through this impactful role with Elpida.
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