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Salary
≈ $86k – $192k per year (Estimated)
Location
In office (Reading, Dublin)
Seniority
Principal · 3+ years exp
Visa
Licensed UK visa sponsor
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 30, 2026. First seen by Alion on Oct 27, 2026. IQVIA scores B on the Alion truth index.

Overview
Company
Impact
Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

Job Overview

Independently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high-quality data management products that meet customer needs. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site Manager, and/or a leadership role in a specific CDM task (e.g. Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.

Essential Functions

  • Client Management: Serve as primary point of contact for customer on data management deliverables
  • Manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies.
  • Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
  • Lead direct negotiations with customer, e.g., timelines, financial, process, resources.
  • Maintain strong customer relationships
  • Ensure open communications with customer and IQVIA management to independently manage and meet contractual obligations
  • undefined
  • Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
  • Provide training and development on data management expertise to junior team members
  • Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders
  • Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
  • Serve as the escalation point for unresolved data issues
  • Independently work with client data managers, vendors, internal team members for resolution
  • Ensure appropriate resources are assigned to meet project deliverables
  • Create and/or review and sign-off on all data management plan (DMP) documents
  • Ensure service and quality meet agreed upon specifications per the DMP and contract/SOW
  • Implement proactive quality management plans across multiple projects/programmes/customer account.
  • Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
  • Continuously look for opportunities to improve service
  • Develop and work with team to implement plan to re-organise and drive change (possibly across a customer account)
  • Ensure timely follow-up and resolution of compliance issues
  • Serve as Subject Matter Expert (SME)
  • Provide leadership and expertise in a specific CDM task or technology
  • Serve as customer site lead for one or more customers
  • Train and mentor junior DTL staff in DM expertise
  • May coordinate the work of more junior DTL staff
  • Independently maintain internal tracking databases and systems
  • undefined
  • Independently manage SOW/budget
  • Review financial reports on a monthly basis and participate in project reviews as requested
  • Identify out of scope tasks and track change orders to completion
  • Participate in pricing discussions across customer account
  • Serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing
  • Independently support RFP process (review RFP documents, pricing, attend bid defense) Other:
  • Independently bring process improvements and solutions to the CDM team/CDM department
  • Lead a focus team or global or local best practice team
  • Communicate lessons learned and/or present in CDM workshop(s)Manage the development and implementation of new technology or tool
  • Present at professional conferences and/or publish articles in professional journals
  • Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
  • Perform other duties as directed by the functional manager

Qualifications

  • Bachelor's Degree Health, clinical, biological or mathematical sciences, or related field
  • 5 years of direct Data Management experience with 3 or more years as a CDM project lead
  • Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients).
  • Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology).
  • Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently.
  • Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
  • Knowledge of operating procedures and work instructions and the ability to apply them in practice.
  • Knowledge of Good Clinical Practices and relevant regulatory guidelines.
  • Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work independently.
  • Comprehensive understanding of clinical drug development process.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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