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This is a great job opportunity for an experienced CTA to work on behalf of an international pharmaceutical company and to join a global team.
De functie / The role
Roles & Responsibilities of the position
The Global Tral Manager CTA supports the Clinical Project Leader and/or Global Trial Manager in the operational aspects of all data generation activities.
-Assists with project management activities, as assigned by the CPL/GTM/TM, during the various phases of a project including start-up, execution and close-out.
-As a member of the Study Management Team for each project assigned, the GTM-CTA is responsible for setting up meetings and maintaining minutes.
-Assists in management of project budgets including Affiliate spend, reconciliation of invoices, final budget, and liaising with Accounts Payable, as necessary
-Manages and updates the Clinical Trial Management System ensuring up-to-date, complete and accurate status at all times.
-Manages and updates the Trial Master File (TMF) and Trial Master Source (TMS) across various phases of a project.
-Maintains project-specific SharePoint sites to ensure availability of all central project documents.
-Ensures investigator and IRB/IEC lists are available for Clinical Study Reports.
-Liaises with external service providers e.g. contract research organization (CRO) as needed.
-Supports GTMs/TMs and Quality Assurance (QA) team with audit findings report and CAPA management.
Het profiel / Your profile
oBachelor"s degree or equivalent.
oExperience in the Pharmaceutical industry or CRO.
oGood organization skills, good written and verbal communication skills
oExcellent independent time management skills
oComputer literacy is required. Proficiency in Microsoft Office applications and use of Internet
oProven ability to plan and track deliverables and timelines
Fluent in English
Het aanbod / The offer
We offer a long term collaboration, full time or 0.8/0.9 FTE and partially home based role