About this role

Initiate and coordinate activities and essential documents management during startup towards the compilation of a high quality Investigator Initiation Package (IIP)
Provide support to resolve issues or concerns and timely escalation of site issues where applicable
Prepare, validate and submit regulatory documents for internal regulatory approval within required timelines
Manage and coordinate with other supporting roles to ensure timely site activation and operational activities
Support the compilation of the Central Investigator Review Board package and submissions to approval of the study
Maintain ongoing contact and communication with the study team and respond promptly to study team and investigator site requests

Minimum 2 years relevant experience in clinical site management
Knowledge of clinical research and development processes
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Must be fluent in local language and in English
Multilanguage capability is preferred

Site Activation Partner – Study Start Up Associate

Key skills