799 million. That's how many lives our products touch. And while we're proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's lives? To provide operational expertise in the mobilization of the organization's commitment to sharing of clinical trial documentation and data sets; to work directly with project teams to create and finalize clinical trial documentation and data sets for disclosure; to support and promote consistency with disclosure policies as set forth by the Clinical Disclosure Office and Data Privacy. 1. Act as subject matter expert for disclosure requirements on submission-related clinical trial documentation and data sets. 2. Support regulatory communication about clinical trial documentation and data sets for disclosure. 3. Support policy-specific scope identification of clinical trial documentation and data sets from submission results. 4. Provide project management for submission team assessment of in-scope documentation for commercially confidential information, critical company information, and potential copyright violation and the corresponding rationale. 5. Perform as needed marking and redaction of clinical trial documentation using appropriate tools. 6. Coordinate and QC vendor results. 7. Provide project management for project team review of vendor results, feedback to vendor, and revision of vendor results.