Data Specialist

Description

· Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities.

· Assist in creating external data transfer agreements, ensuring alignment with Takeda Standards and specifications to support data integration, analysis, and reporting.

· Provide support in setting up infrastructure for external data to flow into Takeda Clinical data pipelines.

· Assist in validation of all 3rd Party Data generated in clinical trials into Takeda Clinical Data pipelines.

· Develop and maintain working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards, and other Study Execution Team members.

· Assist in preparing function for submission readiness and may support Clinical Trial Tools & Technologies (CT3) group in formal inspections or audits.

· Act as a representative for Takeda in interactions with key external partners as part of the Takeda CT3 3rd Party Data Acquisition team.

· Support timely submission and ongoing maintenance of study-related 3rd Party Data Acquisition documentation in TMF.

· Follow procedural documents and assist in reviewing and updating documents to ensure they reflect industry standards and regulatory requirements and include optimal processes.

· Assist in liaising with and reviewing work delivered by external partners (e.g., laboratories, eCOA providers, technology providers) performing services on behalf of Takeda.

· Escalate issues to CT3 leadership as appropriate.