Position Overview
Roles & Responsibilities:
Serve as the subject matter expert for planning, setup, and acquisition of external clinical data at the study level, managing study startup, conduct, and closeout activities.
Create external data transfer agreements, ensuring alignment with company standards and specifications to support data integration, analysis, and reporting.
Provide guidance in setting up infrastructure for external data flow into company clinical data pipelines.
Oversee the validation of all third-party data generated in clinical trials, ensuring accurate integration into company clinical data pipelines.
Develop strong and productive working relationships with key stakeholders, including Clinical Data Management, Clinical Data Engineering, Standards, and other Study Execution Team members.
Support submission readiness efforts and may represent the Clinical Trial Tools & Technologies (CT) group in fo...