Clinical Registry Administrator

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Apply locations: Reading, Berkshire, United Kingdom; Centurion, South Africa

Time type: Full time

Posted on: Posted Yesterday

Job requisition id: R

Clinical Registry Administrator role :

• Provides clinical registry support, oversight, and/or accountability for one or more clinical trials.
• Gathers content and integration requirements for registration records. Establishes expectations for dataset content and structure. Sets timelines and follows up regularly to ensure delivery of all clinical trial disclosure milestones.
• Responsible for submission of approved documents and content to registries worldwide, either directly (e.g., clinicaltrials.gov, EU clinical trial register) or indirectly through local operating company staff.
• Tracks, reports, and documents disclosure records and associated documents in tools and systems used by the clinical registry group.
• Plans, routes, and follows up on disclosure documents with business partners, external partners, and local operating companies to ensure timely and compliant delivery.
• 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 facilitate compliant disclosure planning.
• Ensures deliverables are on time.

Education and Experience Guidelines:

• A minimum of 2 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO, or other clinical development service organization) is required.
• Bachelor's degree in health or science discipline with experience in clinical research.
• Project management and vendor management skills.

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