Study Start Up Associate Ii

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/78yidy

As 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.
Annual leave entitlements
Health insurance offerings
Global Employee Assistance Programme (LifeWorks)
Life assurance
Flexible country-specific optional benefits
Coordinate site start-up and activation activities across assigned studies
Review and approve site essential documents (ICF, FDF, ****, CVs, etc.)
Collaborate with internal Study Startup team, CROs, Clinical Operations, and TAU partners to improve SSU metrics




Ensure SSU standards are consistently applied across projects
Monitor timelines,
Support issue resolution with CROs and Clinical Operations, in partnership with the internal team
Provide feedback on site performance metrics and contribute to eTMF accuracy during start-up
Maintain thorough documentation and communication records for assigned sites
BS degree or international equivalent
2+ years of site start-up experience in pharma, CRO, or relevant vendor
Ability to explain data to support data-driven decision making
Knowledge of clinical study protocols and essential documents
Strong organizational, decision-making, communication, and negotiation skills
Proficiency in Microsoft Excel, Word, and PowerPoint
As a Study Start Up Associate II at ICON, you will lead site initiation and activation efforts, ensuring regulatory compliance and timely de
#J-*****-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/78yidy