Cta - Oncology

• Support day-to-day clinical trial operations across one or more studies
• Maintain and organize Trial Master File (TMF) documentation and track essential study records
• Monitor document status and communicate outstanding items to the study team
• Track study metrics, enrollment, site activity, and clinical supply information
• Assist with vendor, CRO, and site coordination activities
• Support invoice tracking, reconciliation, and study budget administration
• Identify and communicate study issues, risks, or operational concerns to the clinical team
• Assist with review and management of study-related documents and materials
• Ensure compliance with applicable regulations, GCP guidelines, SOPs, and study requirements
• Perform additional clinical operations activities as assigned

• Bachelor's degree in Life Sciences or a related field preferred
• Minimum of 3 years of clinical operations or clinical trial support experience
• Experience supporting clinical studies within the biotechnology, pharmaceutical, medical device, or CRO industry preferred
• Oncology experience required
• Working knowledge of clinical trial processes, documentation, and GCP requirements
• Strong organizational skills with exceptional attention to detail
• Proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint
• Strong written and verbal communication skills
• Ability to manage multiple priorities and work effectively in a collaborative environment

Experience supporting clinical studies within the biotechnology, pharmaceutical, medical device, or CRO industry preferred