Lead clinical studies as a Study Operations Manager II, ensuring seamless execution from startup to close. Bring your expertise in strategic planning and study oversight to drive operational excellence.

As the Study Operations Manager II, you will lead local study teams and manage study activities across multiple regions. You will be accountable for coordinating with Contract Research Organizations and managing country-specific plans, including timelines and budgets. This role includes responsibilities in study startup, recruitment strategies, and ensuring compliance with regulatory submissions.

Key Responsibilities:
• Lead local study team to execute operational plans
• Oversee country-level plans for timelines and budgets
• Manage CRO and site activation processes effectively




• Coordinate communication with internal stakeholders and vendors
• Ensure timely resolution of study and site issues

Requirements:
• Bachelor’s degree with minimum 5 years clinical trial experience
• Master’s degree with minimum 3 years relevant experience
• Preferred scientific or technical degree
• Solid organizational and leadership skills
• Experience in regulatory submission strategies

Drive study operations success and utilize your clinical trial expertise for impactful results as a Study Operations Manager II.
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📌 Clinical Study Operations Manager II (Manitoba)
🏢 Parexel International
📍 Manitoba