Clinical Operations

• Lead and coordinate global study teams to ensure the successful delivery of clinical trials.
• Develop and manage study plans, timelines, budgets, resources, risks, and mitigation strategies.
• Select, manage, and oversee CROs and third-party vendors, including participation in RFP processes and vendor selection.
• Drive study execution from protocol development through study close-out and archiving.
• Identify risks, implement corrective actions, and ensure compliance with quality standards and ICH-GCP requirements.
• Review and contribute to key clinical study documents.
• Facilitate study team meetings and ensure follow-up of actions and decisions.
• Collaborate with cross-functional stakeholders to ensure efficient study conduct and patient recruitment strategies.
• Ensure inspection readiness and support audits and regulatory inspections.
• Maintain oversight of Trial Master File (TMF) completeness and study documentation quality.

Clinical Operations jobs in France

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Global Clinical Project Manager