Digital Health Solutions Lead

IQVIA; Reading; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading global provider of clinical research services seeks a Digital Health Systems Analyst to join their Reading office. The role involves collaborating with business users, overseeing supplier systems, and ensuring compliance with regulatory requirements. Ideal candidates will have experience in the healthcare or pharmaceutical industry, strong analytical skills, and the ability to communicate with various stakeholders effectively. This position offers full-time employment in a dynamic environment focused on innovative clinical solutions.

Qualifications

• Previous experience in CRO, Healthcare, or Pharmaceutical Industry.
• Experience in Computer System Validation (CSV) and audit participation.
• Strong understanding of Clinical Trial SaaS platforms.

Responsibilities

• Collaborate to document requirements for DH capabilities.
• Support validation processes for supplier systems.
• Write and execute detailed test scripts.

Skills

Analytical thinking

Problem-solving skills

Excellent documentation

Stakeholder communication

Detail-oriented

Job description

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• Collaborate with business users to consolidate and document requirements for DH capabilities.
• Support planning and execution of validation and qualification processes for supplier systems.
• Write and execute detailed test scripts with precision and accuracy.
• Review and contribute to System Development Lifecycle (SDLC) documentation, including supplier release notes and change memos.
• Engage with stakeholders across privacy, security, quality, and regulatory functions.
• Participate in audits and inspections, fulfilling documentation and data requests.
• Support data standardization, integration, and ingestion across the DH landscape.
• Oversee supplier systems, managing issues, risks, and escalations as needed.
• Ensure compliance with internal processes and external regulatory requirements.
  
  

Key Responsibilities:

• Collaborate with business users to consolidate and document requirements for DH capabilities.
• Support planning and execution of validation and qualification processes for supplier systems.
• Write and execute detailed test scripts with precision and accuracy.
• Review and contribute to System Development Lifecycle (SDLC) documentation, including supplier release notes and change memos.
• Engage with stakeholders across privacy, security, quality, and regulatory functions.
• Participate in audits and inspections, fulfilling documentation and data requests.
• Support data standardization, integration, and ingestion across the DH landscape.
• Oversee supplier systems, managing issues, risks, and escalations as needed.
• Ensure compliance with internal processes and external regulatory requirements.
  
  

Required Qualifications:

• Previous experience working in the CRO, Healthcare or Pharmaceutical Industry
• Experience in Computer System Validation (CSV) and audit/inspection participation.
• Familiarity with Software Development Life Cycle (SDLC) and GAMP5 methodology.
• Strong understanding of Clinical Trial SaaS platforms/applications.
• Excellent documentation, analytical thinking, and problem-solving skills.
• Ability to manage and communicate with multiple stakeholders effectively.
• Detail-oriented with a strong focus on process and activity execution.
  
  

Preferred Experience:

• Knowledge of systems used by preferred or established suppliers in the clinical trial space.
• Experience supporting system integrations and change control processes.
• Exposure to data governance and digital health data ecosystems.
  
  

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

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Management and Manufacturing

• Industries

  Pharmaceutical Manufacturing

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