Manage a group of oncohaematology trials: evaluation and validation, initiation, routine, and close-out visitsRecruit investigators for participation in clinical trialsNegotiate study budgets with investigatorsCreate and discuss relevant study agreementsPrepare a country-specific ICF in the local languagePartner with Global and Local Trial Managers, Projects Physicians, Site Managers and other trial-related roles to ensure successful site managementControl timelines and recruitment to ensure successful outcome of the projectCommunicate with externalthird party vendorsWhen allocated by study management, submit essentialrequired documents to a central IRB or a country’s central Ethics CommitteeEnsure compliance with the protocol, company SOPs, ICH-GCP and local regulatory requirements, local productivity targetsOrganize and conduct local Investigators’ Meetings