Ref #: 24478

Employment type: Permanent - Full-Time

Location: Chile - Santiago

Posted: 06-Oct-2020


• Coordinates with the clinical project team the distribution, retrieval and review of regulatory documents required for initiation of a clinical trial.
• Assures the accuracy of required clinical trial documents maintained within LSF throughout the clinical trial.
• Generates grant payments requests, maintains tracking tool for each study and resolves payment inquiries from investigator sites.
• Prepares necessary study supplies for clinical trials and processes site requests for shipping supplies, as needed. Maintenance of clinical trial tracking systems.
• Other related duties as assigned.
• Maintaining technology skills to meet the challenges of the evolving electronic documentation era solved by obtaining training on systems updates. Assisting the study teams in meeting timelines.
Solved by working closely with the study team.
• Must have an advance English level.