Job Overview

Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.

Essential Functions

• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions

• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers

• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures

• Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans

• Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned.

• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements

• Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle

• Lead/collaborate/support in QA initiatives/projects for quality, process improvements

• Assist in training of new Quality Assurance staff

• May be required to manage Quality Issues

• May present educational programs and provide guidance to operational staff on compliance procedures

• May host audits/inspections; ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections, as assigned.

Qualifications

• Bachelor's Degree Pref

• 5 years experience in pharmaceutical, technical, or related area, of which 3 years in Quality Assurance Audits. GCP experience. Equivalent combination of education, training and experience.

• Experienced in the conduct of CSR/DM/BIOS clinical trial audits.

• Knowledge of word-processing, spreadsheet, and database applications.

• Extensive knowledge of pharmaceutical research and development processes and regulatory environments.

• Knowledge of quality assurance processes and procedures.

• Strong interpersonal skills.

• Excellent problem solving, risk analysis and negotiation skills.

• Strong training capabilities.

• Effective organization, communication, and team orientation skills.

• Ability to initiate assigned tasks and to work independently.

• Ability to manage multiple projects.

• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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