Leading or supporting operational activities from start-up to close-out for assigned studies and investigator sites.
Initiate and coordinate activities and essential documents management 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.
Manage and coordinate with other supporting roles to ensure timely site activation and operational activities.
Collaborate with in country regulatory group, and provide related/applicable site documents.
Accurately update and maintain clinical trial systems that track site compliance and performance within project timelines.
Identify and resolve investigator site issues.

School diploma/certificate with equivalent combination of education, training and experience
BS/BA or bachelor’s degree in life sciences preferred
Minimum 2 years relevant experience in Clinical Trials environment and clinical site activation
Experience working in the pharmaceutical industry/or CRO is an asset
Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations
Must be fluent in Local language and in English.
Multi-language capability is an asset

Site Activation Partner

Key skills