Vendor Manager IRT

IRT set up, follow up and closure: • Contribution to RFP and SOW • Kick-off/alignment meetings • IRT risk assessment/mitigation plan • IRT microplanning validated • IRT Project Requirements and Data Transfer Specifications • Communication plan, study maintenance plan, IRT user documents • IRT sections of study documents validated (protocol, plans, manuals…) • IRT test plan for patient management aspects (including scripts and data transfers)/ UAT coordination • Study IRT training material • Final documents (including QC check list) for QA release • Approval for IRT go live

About You

At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values.

• Experience: Strong work experience of at least 2+ years in clinical trials

• Skills: This position requires a strong communicator who demonstrates accountability, agility, and an intrapreneurial mindset within complex, cross-functional environments. The ideal candidate will align local and regional strategies, actively listen, and build mutually valuable relationships with diverse stakeholders.