Clinical Registry Coordinator - UK Based

IQVIA; England; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading global provider of clinical research services is seeking a professional to provide clinical registry support and oversight for clinical trials. The ideal candidate will have a minimum of 4 years of relevant experience in clinical development and a bachelor's degree in a health or science discipline. Responsibilities include leading the clinical development team to establish registry expectations and tracking disclosure records. Join us to contribute to innovative medical treatments and improve patient outcomes worldwide.

Qualifications

• Minimum of 4 years in a clinical development environment required.
• Bachelor's degree in Health or Science discipline required.
• Clinical Registry experience preferred.
• Experience in clinical trial or regulatory document management preferred.

Responsibilities

• Provides clinical registry support and oversight for clinical trials.
• Leads the clinical development team to establish registry expectations.
• Tracks and documents disclosure records for clinical registries.
• Assists in maintaining accurate data relevant to the disclosure process.
• Ensures timely resolution of planning issues.

Job description

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.

Qualifications

• 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com