Enable job alerts via email!

Project Specialist - Clinical Registry Coordinator

IQVIA, Inc.

Reading

On-site

GBP 35,000 - 55,000

Full time

14 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking a Clinical Registry Specialist to support clinical trials and manage disclosure processes. In this role, you will oversee the submission of clinical trial documents to various registries, ensuring compliance and timely delivery. Your expertise in project and vendor management will be crucial as you collaborate with business partners and local operating companies. This position offers an opportunity to contribute to innovative medical treatments that enhance patient outcomes globally. If you have a passion for clinical research and a commitment to excellence, this role is perfect for you.

Qualifications

  • 3+ years in clinical development within pharma or CRO environments.
  • Strong project and vendor management skills are essential.

Responsibilities

  • Provide oversight for clinical trials and ensure timely document submissions.
  • Track and report disclosure records in clinical registry systems.

Skills

Clinical Trial Management
Project Management
Vendor Management
Data Integration

Education

Bachelor's degree in health or science discipline

Tools

Clinical Registry Tools

Job description

Essential Functions:

  • 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 3 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

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.