Opportunity Description
General Activities
Manages clinical investigational sites. Trains and provides direction to the investigators and the staff of the sites. Reviews, verifies and ensures that clinical documentation fulfils all protocol, GCP and regulatory requirements and maintains drug accountability.
Clinical Trial Associate
Collects, analyses, manages, updates and keeps control of study documentation. Provides support to investigational sites and CRAs. Reports, uploads and keeps updated information in computerized systems.
Project Manager
Management of clinical projects/programs which implies maintaining direct communication and interaction with sponsors, laboratories and supply chain services providers; tracking and reporting of project progress in all investigational sites; schedule, control and approval of site visits and trip reports, managing the financial aspects of the project; and managing the performance of the staff assigned to the project.
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