Clinical Operations Associate
Core
Provide administrative and operational support to clinical study teams throughout the clinical trial lifecycle, ensuring efficiency, quality, and compliance.
Role type
Junior clinical operations support specialist
Builds
Clinical trial operations and documentation
Domain
Clinical research / Healthcare
Required skills
Clinical research site experience, English fluency, Microsoft Office proficiency, multi-priority management, organizational skills, attention to detail
Preferred skills
Experience as Site Coordinator or Research Coordinator
Technologies
Microsoft Office, electronic study systems, Trial Master File (TMF) systems
Responsibilities
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; Track, collect, scan, file, and process study documents and Case Report Forms (CRFs); Provide limited site-facing support in partnership with Clinical Research Associates
