Clinical Registry Administrator

IQVIA LLC; Reading; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global clinical research provider is seeking a Clinical Registry Administrator in Reading, UK. Responsibilities include oversight of clinical trials and submission of documents to registries. The ideal candidate will have a Bachelor’s degree in health or science, with at least 2 years of relevant experience in the clinical development environment. Strong project and vendor management skills are essential. This full-time role offers an opportunity to enhance patient outcomes in healthcare.

Qualifications

• Minimum 2 years of experience in a clinical development environment required.
• Experience with clinical research necessary.

Responsibilities

• Provide clinical registry support for clinical trials.
• Submit documents to registries worldwide.
• Ensure delivery of clinical trial disclosure milestones.

Skills

Clinical registry support

Project management

Vendor management

Attention to detail

Education

Bachelor’s degree in health or science discipline

Job description

Clinical Registry Administrator page is loaded

Clinical Registry Administrator

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

Time type: Full time

Posted on: Posted Yesterday

Job requisition id: R1496090

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.

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