As a Sr.
Auditor (QA), you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing :Monitoring the collection, processing, and analysis of data for sponsored clinical trialsMonitoring and evaluating Supplier compliance and data qualityTracking corrective actions in relation to monitoring issues and audit findings; escalates as appropriateDeveloping professional relationships with sponsor stakeholdersSupport the planning, management and execution of Supplier Performance Management Services related monitoring activitiesSupport Global Development Operations, Global Study Management, and therapeutic area teams by monitoring to ensure the quality and integrity of processes and data generated by external Vendor / Service SuppliersGather business requirements to develop Pre-Visit letters and design and generate reports in support of supplier monitoring activities (eg, Clin Ops DB, IMS)Plan and conduct monitoring visits as delineated in the annual monitoring planAssist in "in-house monitoring" or "remote monitoring" activities as delegated by management or business needEnsure the quality and integrity of processes and data generated by Suppliers for sponsor clinical trialsAssist in the distribution and archival of key outputs from Supplier Performance Management Monitoring (e.g.
Monitoring Visit Reports)Support key governance forums (e.g.
primary FMTs, charter immersion meetings) and ensure accurate records of oversightOversee workspaces and/or repositories for team collaboration on documents and communication of timelinesSupport supplier management in overseeing monitoring activities through timely development and maintenance of business toolsIdentify and implement new business tools to enhance quality of Supplier Performance Management processes and report informationSupport special projects as identified by management or business needFacilitate execution of supplier surveys and address pertinent business issuesDrive continuous improvement of Supplier Performance ManagementCommunicate with internal and external business partners to identify opportunities for enhancing business operationsYou are :Doctorate / Masters / BA / BS / RN / AD / GEDIf Master's degree, 3 years of directly related experience; if Bachelor's degree, 5 years of directly related experience; if Associate's degree, 10 years of directly related experience; if GED, 12 years of directly related experienceExperience evaluating performance for clinical trial vendorsImaging vendors (required)Technologist or work experience in imaging technology and their application to clinical trials (preferred)What ICON can offer you :Our success depends on the quality of our people.
That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON offers a range of additional benefits.
Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.Our benefits examples include :Various annual leave entitlementsA range of health insurance offerings to suit you and your family's needsCompetitive retirement planning offerings to maximize savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among othersVisit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, diversity, inclusion & belonging are fundamental to our culture and values.
Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities.
We're proud of our diverse workforce and the work we've done to become a more inclusive organization.
We're dedicated to providing an inclusive and accessible environment for all candidates.
ICON is committed to providing a workplace free of discrimination and harassment.
All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements?
We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
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