ppAs a Study Start Up Associate II at ICON, you will lead site initiation and activation efforts, ensuring regulatory compliance and timely delivery.
You will collaborate with internal teams, CROs, and TAU partners to optimize SSU metrics and standardize processes.
You will review essential documents and support issue resolution to keep studies on track.
You join a mission-driven organization that values inclusion, excellence, and innovation in clinical development.
This role offers meaningful impact by shaping how trials start up and scale across sites.
/pulliAnnual leave entitlements /liliHealth insurance offerings /liliGlobal Employee Assistance Programme (LifeWorks) /liliLife assurance /liliFlexible country-specific optional benefits /liliCoordinate site start-up and activation activities across assigned studies /liliReview and approve site essential documents (ICF, FDF, ****, CVs, etc.) /liliCollaborate with internal Study Startup team, CROs, Clinical Operations,



and TAU partners to improve SSU metrics /liliEnsure SSU standards are consistently applied across projects /liliMonitor timelines, /liliSupport issue resolution with CROs and Clinical Operations, in partnership with the internal team /liliProvide feedback on site performance metrics and contribute to eTMF accuracy during start-up /liliMaintain thorough documentation and communication records for assigned sites /liliBS degree or international equivalent /lili2+ years of site start-up experience in pharma, CRO, or relevant vendor /liliAbility to explain data to support data-driven decision making /liliKnowledge of clinical study protocols and essential documents /liliStrong organizational, decision-making, communication, and negotiation skills /liliProficiency in Microsoft Excel, Word, and PowerPoint /li /ulpAs a Study Start Up Associate II at ICON, you will lead site initiation and activation efforts, ensuring regulatory compliance and timely de /p /p #J-*****-Ljbffr

📌 Study Start Up Associate Ii (Bardi)
🏢 Experteer Italy
📍 Bardi