ICON plc
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Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Clinical Operations Study Lead at ICON, you'll manage projects, lead teams, develop project plans, and mentor staff to ensure successful project execution in clinical settings.
Healthtech • Biotech • Pharmaceutical • Manufacturing
Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Senior Issue Lead manages Major Quality Event investigations, coordinates audits, ensures compliance with GCP standards, and trains Issue Leads. This role involves root cause analysis, process improvement, and leading quality assessments.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Third Party Quality Lead manages third-party quality risks in clinical operations, ensures GCP compliance, and oversees vendor performance and quality systems.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Quality ICM Issue Lead oversees quality event case management, leading investigations, notifications, root cause analysis, and process improvements within clinical development.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Global Study Manager, you will lead project execution, manage cross-functional teams, and develop strategies to meet project goals in the healthcare sector.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Global Study Manager will lead project management activities, develop plans, guide teams, and collaborate with stakeholders to achieve project goals in oncology clinical research.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Site Activation Partner, you will manage the initiation of clinical trials, ensuring compliance and supporting regulatory submissions while collaborating with stakeholders.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Global Study Manager oversees project management activities in oncology, ensuring successful project execution by leading teams, developing project plans, and maintaining stakeholder communication.