Clinical Registry Administrator

IQVIA, Inc.; Reading; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading clinical research organization in the UK seeks a Clinical Registry Administrator to support clinical trials. Responsibilities include overseeing registry submissions, ensuring compliance, and tracking documentation. Candidates should have 2+ years in a clinical development environment and a Bachelor's in a health or science discipline. Strong project and vendor management skills are necessary for success in this role.

Qualifications

• Minimum of 2 years of relevant pharmaceutical/scientific experience in a clinical development environment.
• Experience in clinical research.
• Strong project management and vendor management skills.

Responsibilities

• Provides clinical registry support for one or more clinical trials.
• Tracks, reports, and documents disclosure records and associated documents.
• Ensures timely resolution of planning issues for compliant delivery.

Skills

Clinical trial oversight

Data integration requirements

Project management

Vendor management

Education

Bachelor's degree in health or science discipline

Job description

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. - Set timelines and follow-up regularly to ensure delivery of all clinical trial disclosure milestones.
• Responsible for submission of approved documents and content to registries worldwide, either directly such as for clinicaltrials.gov or the EU clinical trial register, or indirectly by providing to the local operating company staff for subsequent submissions to local registries
• Responsible for tracking, reporting and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group
• Responsible for planning, routing, and follow-up of disclosure documents with business partners, external partners, and local operating companies, ensuring timely and compliant delivery of these documents
• Assisting 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.

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