Clinical Registry Coordinator - UK Based

IQVIA; England; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading clinical research firm in the UK is seeking a Clinical Registry Coordinator to provide oversight for clinical registry support and ensure timely and compliant processes. The ideal candidate will have at least 4 years of relevant experience in a clinical development environment, preferably with clinical registry experience. This role requires strong communication skills and a Bachelor's degree in a Health or Science discipline. If you are passionate about improving patient outcomes, this opportunity may be for you.

Qualifications

• Minimum of 4 years of relevant pharmaceutical/scientific experience.
• Experience in clinical research preferred.
• Clinical registry experience preferred.

Responsibilities

• Provides oversight and accountability for clinical registry support.
• Leads internal and external partners to align clinical registry expectations.
• Ensures timely resolution of planning issues for compliant delivery.

Skills

Pharmaceutical knowledge

Clinical research

Data tracking

Communication skills

Education

Bachelor's degree in Health or Science discipline

Job description

Clinical Registry Coordinator - UK Based page is loaded## Clinical Registry Coordinator - UK Basedlocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R1519423**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 atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.