Clinical Registry Administrator - UK based

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

Job summary

IQVIA, un fournisseur mondial de services de recherche clinique, recherche un Administrateur de Registre Clinique. Vous serez responsable du soutien pour plusieurs essais cliniques, de la soumission de documents à des registres internationaux, tout en maintenant des délais stricts pour une conformité totale. Avec un minimum de 2 ans d'expérience dans un environnement de développement clinique et un diplôme en santé ou en science, vous aurez un impact direct sur le développement de traitements médicaux innovants.

Qualifications

• Minimum de 2 ans d'expérience en développement clinique.
• Expérience en gestion de projet est souhaitable.
• Compétences en gestion des fournisseurs requises.

Responsibilities

• Fournit un soutien et une responsabilité pour les essais cliniques.
• S'occupe des soumissions de documents aux registres mondiaux.
• Assure la résolution des problèmes de planification.

Skills

Gestion de projet

Gestion des fournisseurs

Education

Baccalauréat en santé ou discipline scientifique

Job description

Clinical Registry Administrator role :

• Provides clinical registry support, oversight, and accountability for one or more clinical trials.
• Gathers content and integration requirements for registration records, establishes expectations for dataset content and structure, and sets timelines with regular follow-up 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 for subsequent submissions.
• Tracks, reports, and documents disclosure records and associated documents using tools and systems employed 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 (source) data relevant to the disclosure process.
• Ensures timely resolution of planning issues to facilitate compliant disclosure planning.
• Ensures all deliverables are completed 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 a 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 improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com