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Data Strategy Director, multiple EU locations

4 mesi fa

Rome, Italia PAREXEL A tempo pieno
When our values align, there's no limit to what we can achieve.At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.This role can be flexibly based in selected EU locations Picture Yourself At Parexel:The Regional Head, Scientific Data Strategy is a Director level job responsible for identifying and implementing innovative access to real-world scientific data (RWD) within their region of both broad and deep patient clinical domains.

This includes determining the best methods for partnering with health systems, data vendors, national/regional patient registries, disease-specific registries and other novel sources of real-world scientific data.

This is an advanced role that requires leadership competencies, accountability, relationship management skills and business acumen.

Individuals must ensure that the application of RWD from the region for a given solution is fit-for-purpose and is used in a manner compliant with the data use agreement and applicable law.The Head, Europe RWD Strategy leads the Europe team with high visibility and sales capabilities as we have many clients throughout Europe with requirements to support RWE studies using registry, EMR, and other RWD sources. This role offers keen insights into innovative methodologies such as AI use in RWE, PASS and therapy area applications using RWD as well as specific expertise in EMA regulatory guidance to chart a successful path forward for generating evidence from RWD.What You'll Do At Parexel:Scientific and Real-World Data Asset AccessResponsible for the execution of a global RWD acquisition strategy within the regionRecognize gaps in Parexel’s scientific and real-world data coverage.

Identify, assess, and recommend options to expand access to RWD and scientific data to fill gaps in Parexel’s coverage within the regionPerform return-on-investment assessments that inform decision-making on whether to strategically partner with select data providersOperate governance frameworks for regional RWD partners and suppliersResponsible for specifications being up-to-date in the data catalog (e.g., new functionality), as well as training and use across business partnersEnsure that data access and use is fully operationalEvolve regional data acquisition with business partner strategy and needsMonitor KPIs used to ensure impactful use of data.

Remediate to deliver return-on-investment as requiredVendor / Provider managementMonitor partner capabilities and services, making recommendations on ways in which the partnership can be strengthened (e.g., improve direct access, feasibility turnaround)Work with Procurement/LRM to establish/manage qualification, due diligence and contractingFollow up on how projects are going and what can be improved in terms of the PXL-partner relationshipSuppliers at minimum to include EMR / EHR; claims; pharmacy; lab, specialty data such as biomarker, genetic, and imaging; registries; clinical outcomes assessments, investigators or expert networks and similar sources of patient data beyond randomized clinical trial dataInfrastructure & Platform DesignPartners with technology teams to ensure region-specific requirements for system architecture are metContribute to descriptive content that can be used in capability presentations, proposals, protocols/SAPs, study reports, etc.Identifies and surfaces regional observations and trends that can inform further growthRelationship ManagementDevelop and maintain working relationships with SDO core solutions teams and functional teams, Parexel business partners, clients and vendors, providers; at minimum, Legal and Risk Management, Procurement, Data Privacy, Project team personnelIdeal candidate will possess:10+ years of experience with the ability to demonstrate the following:In depth understanding of the clinical research process and business, medicines and medical device development, healthcare market and related sectorsBroad cross-functional experience in the healthcare, scientific and real-world data environmentExperience with major patient data models (e.g. CDISC, OMOP, LOINC, FHIR, MEDra, SnoMED etc.)Demonstrated ability to apply scientific or real-world data solutions to address clinical or commercial questions and needsExperienced in budgets and cost evaluation of RWD based solutionsUnderstanding of project management principlesMaster’s degree in biomedical informatics, public health, data science, life sciences or related fieldAdvanced degree (or equivalent experience) in biomedical informatics, public health, data science, life sciences or related field desiredEffective translation of strategy into executable plansLeadership skills in an evolving environment – change managementExcellent oral and written communication skillsExcellent customer focus (internal and external)Excellent interpersonal skillsExperienced in establishing meaningful external partnerships & collaborations with health systems, vendor companies, and individual contributors within the regionAbility to manage multiple projects and prioritiesAbility to identify where regulated requirements applyTechnical skills preparing and processing RWD for application and analysisLeadership decision-making commensurate with position senioritySummaryLocation: United Kingdom-Sheffield-Remote; Spain-Remote; Italy-Remote; Poland-Remote; Romania-Remote; Ireland-RemoteType: Full time