Kelly Vaillant

Global Head (Sr Director), Center of Excellence & Innovation @MMS

Thousand Oaks, CA, US
EMAILS
k••••••••@mmsholdings.com
MOBILE NUMBERS
+18•••••••27

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WORK HISTORY

Jan 2021 — Present

Global Head (Sr Director), Center of Excellence & Innovation @MMS

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US

Responsible for ensuring the organization is focused on delivering exceptional technology enabled services and solutions along with industry best practices & process, knowledge management and performance measurement. • Leads corporate innovation and the development of innovation strategy to enhance MMS services by generating creative ways to improve cost, quality and delivery leveraging technology and best practices. This includes a focus on: o Operational Strategy o Service Maturity o Innovation & Automation o Technology development, adoption, continuous improvement o Cross functional Integration and process alignment• Ensures operational excellence across all Service/Functional areas and across all Technology Solutions.• Leads the collection evaluation of performance measurements (e.g, cost, quality, and delivery).

EDUCATION

N/A

Amgen

Executive Development Leadership Training

N/A

University of Alberta

BSc, NeuroPsychology

SKILLS

Engaging Public SpeakerTherapeuticCross-Functional Team LeadershipSituational AnalysisTrends in OutsourcingContractingSupportive CareClinical DataMentoringTeam BuildingRemote Data CaptureClinical OperationsClinical Data ManagementClinical Trials Disclosure (Ctd)BudgetInnovationStudy EnrollmentSite/Study FeasibilityRfiClinical Research OrganizationSix SigmaProcess OptimizationStrategic PartnershipsSoftware Validation (Iq,Oq,Pq)Performance MetricsProject ManagementBiotechnology IndustryRfpClinical DatabaseStandardsOperations ManagementRoi OptimizationCommunicationCdmData HandlingOncologyElectronic Data CaptureData Flow OptimizationVendor ManagementPartnering

ABOUT KELLY VAILLANT

I am passionate about improving the lives, quality of life, and well-being of patients who are in desperate need of the products and treatments being developed by the companies I have been a part of and work with. Every one of us has had the unfortunate experienced of seeing a loved one, a friend, a colleague suffer with the pain, frustration, and the anxiety of illness. The feeling of hopelessness, the fear of the unknown, and the feeling of absolute helplessness is heartbreaking. I joined the pharma and biotech industry to try and change this – or at least help in some small way. During my career, I have had the opportunity to be a leader and innovator across various areas in clinical development. I have built, grown, and led global functions in the areas of Clinical Data Management, Clinical Operations & Project Management, Clinical Trial Disclosure & Data Transparency, and Clinical Systems. I have extensive experience leading and facilitating global operations, vendor/alliance management, leading and facilitating cross-functional groups/initiatives and executive strategic committees, and developing (or improving) and implementing processes and technologies to facilitate clinical development and clinical trial operations.My focus is on creating and implementing the most effective, efficient, and cost-effective approaches to address the myriad of challenges faced during the development of new products and treatments. I am a Six Sigma Green Belt, was voted Clinical Data Management Chair for PhRMA in 2008 and am a founding member of CDISC. With 20+ years of experience I am just as passionate about my work today, if not more so, than I was on day one. If I can in some small way contribute to improving the outcome, lessen the pain and suffering, improve the quality of life, or allow patients and their loved ones some precious extra time together… I would consider myself successful.

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