Associate Director, Clinical Study Management, EMEA/LATAM
Core
Oversee execution of clinical trials in oncology and other therapeutic areas across EMEA and LATAM regions, ensuring compliance with regulations and delivering studies within timelines and budget.
Role type
Senior IC Clinical Study Management Director
Builds
Clinical study deliverables and operational excellence for oncology/neuroscience drug development
Domain
Biopharmaceuticals / Clinical Operations
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Global clinical trial management (Phases I–IV), ICH-GCP and regional regulatory knowledge, vendor management, budgeting and resource planning, team leadership and hiring, cross-functional collaboration
Preferred skills
Fluency in multiple EMEA/LATAM languages, experience with microRNA/protein-target discovery platforms
Technologies
Veeva TMF, clinical supply management systems
Responsibilities
Manage trial deliverables and timelines across assigned protocols; ensure studies comply with ICH-GCP and regional guidelines; manage ancillary vendor relationships and performance; lead regional Clinical Operations Study Management personnel; provide regular progress updates to stakeholders; oversee clinical supply and import/export requirements
Seniority
Director, hands-on leadership with team building
