Study Start Up Associate II

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/791knc

In this role you lead the initiation of clinical trials, ensuring regulatory compliance and supporting the advancement of new treatments. You collaborate across the Study Startup team, CROs, and Clinical Operations to optimize site activation timelines and maintain accurate documentation. You will monitor site performance, address activation delays, and ensure eTMF quality. This position offers the chance to impact trial timelines and improve SSU processes in a values-driven environment.

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Coordinate site start-up and activation activities and deliverables

Collaborate with internal Study Startup team, CROs, Clinical Operations, and TAU partners to improve SSU metrics

Ensure adherence to SSU standards across projects





Identify and elevate potential site activation delays

Track actions and communications to meet study/site timelines

Resolve escalated issues in partnership with CROs and Clinical Operations

Provide feedback on site performance metrics to management

Ensure accuracy and completeness of the eTMF for assigned sites during start-up

BS degree or international equivalent

2+ years of experience in clinical research Site Start Up within pharma, CRO, or relevant vendor

Ability to translate data into informed decisions

Knowledge of clinical study protocols and essential documents

Strong organizational, decision-making, communication, and negotiation skills

Proficiency in Microsoft Excel, Word, and PowerPoint

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/791knc