OverviewAs a Site Contracts Specialist you'll own the contract lifecycle for clinical studies, from drafting to finalization, within Medpace's Site Contracts Team in Italy. You will negotiate within approved templates, assess risks, and coordinate with internal teams to align site startup activities with contractual timelines. You'll stay current on local regulatory requirements affecting contracts and support cross-functional touchpoints to enable study start-up. This role offers growth in a globally respected CRO with a patient-focused mission and impact on trial execution.ResponsibilitiesDraft, review, negotiate, and finalize clinical study agreements and related legal documentsNegotiate within client-approved templates and parametersIdentify legal, financial, and operational risks and elevate when neededProvide recommendations and alternative resolutions during negotiationsCoordinate with internal functions to align site startup activities with contractual timelinesMaintain up-to-date knowledge of applicable local regulations affecting contractsQualificationsBachelor degreeAt least 1 year of relevant work experienceStrong Italian and English written and spoken communication skillsStrong attention to detailPrior contract negotiation experience preferred but not requiredBenefitsFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
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