Aktis Oncology

Clinical Operations

• Support the planning, execution, and documentation of clinical trials involving radiopharmaceutical agents
• Support day-to-day operations of clinical trial conduct
• Organize and maintain tracking systems and set up metrics and tools from study start-up to close-out
• Track enrollment, monitoring visits, essential documents, and other study activities
• Assist with development and review of protocols, ICFs, and clinical study plans
• Schedule and coordinate study meetings, materials, and agendas
• Record and disseminate study decisions and action items
• Assist with creation, collection, and review of regulatory and study documents
• Coordinate with CROs, vendors, and clinical sites
• Compile study status reports and metrics for internal stakeholders
• Perform ongoing quality-control checks of study documentation and eTMF
• Assist in audit preparation and resolution of audit findings
• Ensure inspection readiness
• Report to the Senior Director, Clinical Operations and work under the direction of the Clinical Trial Manager or Clinical Operations Lead

Explore Senior Clinical Trial Associate – Clinical Ops at Aktis Oncology. Review requirements and application details.

Open roles

Senior Clinical Trial Associate – Clinical Ops