Clinical Operations Associate

• Support clinical study teams with administrative and operational tasks
• Manage site payments and clinical trial supplies
• Maintain and organize essential study documentation within electronic systems
• Perform Trial Master File (TMF) related activities to support inspection readiness
• Track, collect, scan, file, and process study documents and Case Report Forms (CRFs)
• Provide limited site-facing support in partnership with Clinical Research Associates
• Work closely with Clinical Research Associates and project teams throughout the clinical trial lifecycle

• Previous experience working at a clinical research site (Site Coordinator, Research Coordinator, or similar roles)
• Fluency in English is required
• Proficiency with Microsoft Office applications
• Ability to manage multiple priorities in a fast-paced environment
• Strong organizational skills and attention to detail
• A university degree in a healthcare, life sciences, or related field

• Continuous learning and career development opportunities
• Flexible working arrangements
• Healthy work-life balance
• Collaborative, diverse, and supportive global team
• Exposure to a wide range of clinical operations activities and career paths