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• Provides clinical registry support, oversight, and/or accountability for one or more development programs for clinical trials.
• Takes a leadership role with the clinical development team and other internal and external partners to establish, align, and confirm clinical registry expectations for assigned trial(s).
• Responsible for submission of approved documents and content to registries worldwide. Submissions are made by the Clinical Registry Administrators.
• Responsible for tracking, reporting, and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group.
• Assists business partners, external partners, and local operating companies in maintaining accurate and correct (source) data relevant to the disclosure process.
• Ensures timely resolution of planning issues to ensure compliant delivery of the disclosure planning.
• Ensures deliverables are on time.

Qualifications