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IQVIA

Runs drug trials and sells health data to pharma

Senior QA Auditor

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDurham, NC, USAIn-person

About the Job

Requirements

  • Five years of experience in a pharmaceutical, technical, or related area, including three years in Quality Assurance; GXP experience is required.
  • 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.
  • Interpersonal skills; problem-solving, risk analysis, negotiation, training, organization, communication, and team orientation skills.
  • Ability to initiate assigned tasks and work independently, manage multiple projects, and establish and maintain effective working relationships with coworkers, managers, and clients.

Responsibilities

  • Plan, schedule, conduct, report, and close audit activities in countries involved with IQVIA contracts to assess compliance with applicable regulations and guidelines, customer requirements, IQVIA standard operating procedures, and project-specific instructions.
  • Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers.
  • Interpret regulations, guidelines, compliance status, policies, and procedures for project teams.
  • Consult with customers and monitors on audit observations and the formulation of corrective action plans.
  • Manage quality issues.
  • Present educational programs and guide operational staff on compliance procedures.
  • Review and approve investigations, root cause analyses, corrective action and preventive action plans, and effectiveness check plans; track them through closure for quality events arising from quality issues, audits, inspections, or similar quality assurance activities.
  • Provide quality assurance consultancy for clients within budget and established timelines.
  • Evaluate policies and procedures for compliance with applicable regulations and guidelines and recommend continuous process improvements to management.
  • Host audits and inspections, ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections.
  • Perform GLP archivist duties when needed.
  • Manage or oversee quality-event updates in the electronic quality management system and/or maintain the system and support the audit lifecycle.
  • Lead, collaborate on, or support quality assurance initiatives and process-improvement projects.
  • Assist in training new Quality Assurance staff.

Desired Qualifications

  • A Bachelor's degree is preferred.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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