27 ott - Monza
Psi Cro
pIn this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You’ll monitor startup timelines, optimize processes, and contribute to a global pharmacovigilance-minded mission. This position blends hands-on coordination with process improvement in a hybrid Milan setting, offering growth within a patient-focused pharmaceutical environment. /pullibase salary 31,700 – 40,150 gross annual salary /lilibonus /liliincentive plans /liliother benefits may apply /liliSupport site identification and selection process /liliCollect and review documents for ethics and regulatory review and approval /liliPrepare site document packages for drug release to clinical sites /liliPrepare and negotiate site contracts and budgets /liliCommunicate with project teams, investigative sites,
review bodies, vendors, and clients regarding startup matters until site activation /liliMonitor startup metrics and timelines /liliCoordinate initiatives for startup process improvement, analyze best practices and challenges /liliCollege/University degree or equivalent education/experience /liliAt least 1 year of industry experience in clinical research and/or at least 1 year of Study Startup experience in Italy /liliFull working proficiency in English /liliStrong communication and organizational skills /liliAbility to negotiate and build relationships at all levels /lilicommunication /liliorganizational skills /liliethics and regulatory submission /lilisite activation processes /lilicontract and budget negotiation /li /ul #J-18808-Ljbffr
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