The Executive Director (ED) is the Clinical Operations lead in a country/cluster and is responsible for execution of all Clinical Trials in scope for Global Clinical Trial Operations (GCTO) country operations
Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection ready studies is essential
The position is accountable for trial quality and audit responses and completion of CAPAs
Ensures a single point of contact for managing clinical trial execution in all its aspects across phases in scope of GCTO within the country/cluster
Supports the regional GCTO leadership team, leading strategic development of their country/ cluster to deliver clinical trials as per global clinical research pipeline requirement
Strategic country/ cluster representative for initiatives at all levels of the organization.
Build and lead the team to effectively manage resources ensuring appropriately skilled and high performing team to effectively deliver the portfolio across therapy areas and achieve on agreed GCTO, GCD, and Research and Development objectives

10 years or more experience in Clinical Trials
5 years or more people management experience
Experience in Clinical Trial Operations gained from working at hospitals and/or research institutions, recognized clinical trial suppliers/vendors, reputable CRO(s) and/or a Sponsor environment working on multi-phase, multi-therapeutic and clinical trials from study initiation to completion and associated regulatory submission and inspection preparation
Complete understanding of ICH GCP and Global/Regional/Local regulatory requirements is required
Strong Communication skills requiring proficiency in written and spoken English and preferably local language

medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days

Executive Director, Global Clinical Trial Operations, Oncology

Key skills