Clinical Registry Administrator - UK based at IQVIA

Reading, England, United Kingdom

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

NoVisa

Pharmaceutical, Clinical Research, CROIndustries

Requirements

Minimum of 2 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO or other clinical development service organization)
Bachelor’s degree in health or science discipline with experience in clinical research
Project management and vendor management skills
UK based (role not eligible for UK visa sponsorship; only candidates based in listed location/s considered)

Responsibilities

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
Submits approved documents and content to registries worldwide, either directly (e.g., clinicaltrials.gov or EU clinical trial register) or indirectly by providing to local operating company staff for local submissions
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 ensure compliant delivery of disclosure planning
Ensures deliverables are on time

Skills

Key technologies and capabilities for this role

Clinical Registry ManagementClinicalTrials.govEU Clinical Trial RegisterProject ManagementVendor ManagementClinical ResearchDocument SubmissionDisclosure TrackingData Management

Questions & Answers

Common questions about this position

Is visa sponsorship available for this role?

No, this role is not eligible for UK visa sponsorship.

What experience is required for this position?

A minimum of 2 years of relevant pharmaceutical/scientific experience in a clinical development environment is required, along with a Bachelor’s degree in health or science discipline with experience in clinical research.

What skills are needed for the Clinical Registry Administrator role?

Project management and vendor management skills are required.

Where must candidates be based to apply for this job?

Only candidates based in the listed UK location/s will be considered; applications from candidates based outside of these locations will not be considered.

What education is required for this role?

A Bachelor’s degree in health or science discipline with experience in clinical research is required.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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