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Fortrea

Senior Manager, IT Quality and Compliance

Posted 10 Days Ago
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In-Office or Remote
Hiring Remotely in Durham, NC
Senior level
In-Office or Remote
Hiring Remotely in Durham, NC
Senior level
Leads global IT quality and compliance activities, including audits, risk assessments, controls, validation, CAPA and quality-event management. Oversees documentation, governance, regulatory compliance, supplier assessments, training and IT project support. Partners with business, QA and IT teams to ensure timely audit responses and remediation. Manages and develops professional staff while supporting regulated pharmaceutical and drug-development environments.
The summary above was generated by AI

Reporting to the Director, Global IT Quality and Compliance (IT Q&C), the Senior Manager, IT Quality and  Compliance is a member of the Global IT Quality and Compliance leadership team and responsible for  assisting the Director in the execution, operational management, and performance of one or more of  the disciplines of the IT global controls framework, program management, IT risk assessment, IT audit  management and M&A support. The Senior Manager is the interface of Fortrea IT to our clients, customers, study sponsors and Inspectors. As in the interface, you will also work with the various IT groups to 
obtain answers to audit queries and to ensure proper follow-up and on-time completion to IT Quality  events.

The Senior Manager will also facilitate and guide the career growth and development of professional level staff.


Summary of Responsibilities:

  • Lead internal business and IT partners (manage IT involvement) in audits (client, regulatory, and QA).
  • Coordinate, review and complete contract reviews, client questionnaires, requirements for proposals, and other compliance initiatives as they impact IT.
  • Point of contact for IT audit support resources and ensure appropriate IT audit support levels.
  • Tracking, planning and reporting of audit support metrics to ensure appropriate resourcing levels.
  • Lead in the management and execution of one or more components of the overall IT Quality program globally.
  • Represent IT Quality on global IT projects and committees serving as subject matter expert and/or provide oversight to guide business units on how to comply with statutory and develop and maintain formal documentation including policies, standards, and procedures, consistent with corporate, legal and regulatory requirements as well as industry standard best practices.
  • Represent in key IT Governance teams representing IT quality interests (i.e. system validation, infrastructure controls, risk management, policy compliance, etc.)
  • Triage of Audit Quality Events (QE) to ensure appropriate IT Ownership
  • Monitoring IT QEs and CAPAs, provide guidance and work with owners to ensure appropriate and complete actions with on-time closure.
  • Recommend proper controls for the Company's computer systems to ensure the reliability of applications and infrastructure, as well as the integrity of data and safety of subjects.
  • Deliver technology, standards, and processes in accordance with department objectives and goals.
  • Partner with Corporate, QA, and IT Client Engagement and SLC functions to assess and leverage supplier information for validation activities.
  • Lead a team by providing clear articulation of direction and expectations.
  • Provide coaching and support to direct reports in the creation of robust development plans to grow leadership skills that meet succession needs.
  • Educate and trains IT staff, business associates, and IT Project Leads as to the IT Quality Compliance and validation methodology, and their respective responsibilities. Create training  materials and provide training opportunities for IT Quality and Compliance and computer  system validation issues across business units.

Qualifications (Minimum Required):

  • 8 years experience working with in an audit/compliance function, 5 years of which focused on  IT and/or Data Management.  
  • Must have experience working within a CRO/Clinical Industry
  • Strong knowledge of the audit process (i.e. preparation, performance, reporting, follow-up and closure) and audit program management  
  • Prior experience in heavily regulated environments such as financial (SOX) or pharmaceutical (GxP) industries 
  • Knowledgeable of regulatory compliance requirements in pharmaceutical and drug development industries in USA, EU and APAC
  • Familiar with various validation methodologies (SDLC) and their implementation in an IT organization
  • Experience working in a team oriented, collaborative environment.  

Learn more about our EEO & Accommodations request here.

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