Responsible for leading or supporting operational activities from start-up to close-out for assigned studies and investigator sites
Ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and sponsor standards
Initiate and coordinate activities and essential documents management towards the compilation of a high-quality Investigator Initiation Package (IIP) leading to approval for sites initiation
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, as well as in countries where parallel submissions are required
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 – FSP

Key skills