Clinical Registry Coordinator - UK Based
Essential Functions
- 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.
- A minimum of 4 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 is required with experience in clinical research
- Clinical Registry experience preferred.
- Experience working on a clinical trial or regulatory document management preferred.
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