Study Startup Specialist I
In 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.base salary 31,********,150 gross annual salarybonusincentive plansother benefits may applySupport site identification and selection processCollect and review documents for ethics and regulatory review and approvalPrepare site document packages for drug release to clinical sitesPrepare and negotiate site contracts and budgetsCommunicate with project teams, investigative sites,
review bodies, vendors, and clients regarding startup matters until site activationMonitor startup metrics and timelinesCoordinate initiatives for startup process improvement, analyze best practices and challengesCollege/University degree or equivalent education/experienceAt least 1 year of industry experience xysqume in clinical research and/or at least 1 year of Study Startup experience in ItalyFull working proficiency in EnglishStrong communication and organizational skillsAbility to negotiate and build relationships at all levelscommunicationorganizational skillsethics and regulatory submissionsite activation processescontract and budget negotiation#J-*****-Ljbffr
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.base salary 31,********,150 gross annual salarybonusincentive plansother benefits may applySupport site identification and selection processCollect and review documents for ethics and regulatory review and approvalPrepare site document packages for drug release to clinical sitesPrepare and negotiate site contracts and budgetsCommunicate with project teams, investigative sites,
review bodies, vendors, and clients regarding startup matters until site activationMonitor startup metrics and timelinesCoordinate initiatives for startup process improvement, analyze best practices and challengesCollege/University degree or equivalent education/experienceAt least 1 year of industry experience xysqume in clinical research and/or at least 1 year of Study Startup experience in ItalyFull working proficiency in EnglishStrong communication and organizational skillsAbility to negotiate and build relationships at all levelscommunicationorganizational skillsethics and regulatory submissionsite activation processescontract and budget negotiation#J-*****-Ljbffr