Clinical Trials Project Manager Remote
Remote / Online - Candidates ideally in
Repentigny, Lanaudière, Province de Québec, Canada
Listed on 2026-07-10
Repentigny, Lanaudière, Province de Québec, Canada
Listing for:
Elpida Therapeutics
Full Time, Remote/Work from Home
position Listed on 2026-07-10
Job specializations:
-
Research/Development
Clinical Research, Regulatory Compliance Specialist
Job Description & How to Apply Below
Elpida Therapeutics seeks a Clinical Trials Project Manager to lead global clinical trials remotely from Canada. Ensure timely execution and compliance while enriching children's lives with rare diseases.
In this full-time, contractor role, you will manage international clinical trials for rare disease programs. You'll oversee project timelines, budgets, and collaborate with stakeholders such as hospitals and CROs. Your work will directly impact patients and families affected by ultra-rare diseases.
Key Responsibilities:
• Lead day-to-day management of clinical trials globally
• Develop project plans, timelines, and risk registers
• Coordinate activities with investigators, hospitals, and vendors
• Manage patient enrollment strategies and communications
• Ensure compliance with regulatory standards and commitments
Requirements:
• 5+ years of clinical trial management experience
• Strong knowledge of ICH-GCP and clinical research regulations
• Experience with study timelines, budgets, and vendors
• Excellent communication and organizational skills
• Authorized to work in Canada
Utilize your expertise to enhance clinical trials and support impactful therapeutic developments for children in need.
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