Lead Phase I–IV clinical trials remotely from Quebec, applying clinical project management expertise and coordinating cross-functional teams across global time zones.

As a Project Manager at Worldwide Clinical Trials, you will oversee studies from start-up through close-out. You will align resources, plans, budgets, and deliverables with client expectations. The role combines clinical research knowledge, risk management, and operational leadership across matrix teams.

Key Responsibilities:

- Lead cross-functional teams and coordinate external clinical trial partners
- Own study plans from start-up through close-out
- Oversee project resources, finances, timelines, and quality
- Anticipate risks and implement contingency or recovery strategies




- Build client relationships and drive delivery improvements

Requirements:

- Degree in life sciences or equivalent education and experience
- At least five years of clinical pharmaceutical industry experience
- Knowledge of clinical project management, ICH Guidelines, and GCP
- Solid leadership, planning, organizational, and problem-solving skills
- English and French proficiency with travel eligibility

Apply clinical trial leadership, client partnership, and risk management expertise to Phase I–IV studies at Worldwide Clinical Trials.

📌 Clinical Project Manager Rare Disease (Quebec City)
🏢 Worldwide Clinical Trials Canada
📍 Quebec City