Clinical Registry Coordinator - UK Based

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

Job summary

A leading global clinical research provider is seeking an individual with a strong background in clinical development to provide registry support and oversight. The ideal candidate will have a minimum of 4 years of experience in a pharmaceutical or clinical environment, along with a relevant Bachelor's degree. Responsibilities include leading the clinical development team, ensuring compliance, and maintaining accurate data for clinical trials. This position offers the opportunity to contribute to the advancement of innovative medical treatments.

Qualifications

• Minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment.
• Experience in clinical research is required.
• Clinical Registry experience is preferred.

Responsibilities

• Provide clinical registry support and oversight for development programs.
• Lead the clinical development team to establish clinical registry expectations.
• Track and report disclosure records and associated documents.

Skills

Clinical development experience

Data accuracy maintenance

Project management

Leadership skills

Education

Bachelor’s degree in Health or Science

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