Clinical Trial Administrator (CTA)

Our client, an international company, that provides its activity in Clinical Research, is looking for Clinical Trial Administrator

Key responsibilities:

• Provides support to a project team including maintenance of documentation, document tracking and information retrieval. 
• Assists with general administrative functions as required. 
• Maintains and manages data entry into designated tracking systems in accordance with project requirements, including collection of information from designated team members. 
• May be assigned primary responsibility for preparation and management of documentation and reports. 
• Serve as a central contact for communications/correspondence and associated documentation. 
• May be responsible for collection of regulatory documents required for the project start up. 
• Assists with and/or coordinate management of project's data flow. 

Requierements to out perfect employee:

• University degree, health-science related (e.g. medicine, pharmacology, biology etc.) is strongly preferred. 
• Must be able to demonstrate effective time-management skills by prioritizing workload.
• Good interpersonal skills, effective verbal and written communication, the ability to work within a team setting are also required. 
• Must be flexible and results orientated. 
• Must also possess the ability to pro-actively identify and solve problems. Should have a well-organized working style. 
• Intermediate English and computer literacy (at least MS Word, MS Excel, MS Outlook) are required. 

Working conditions:

• official employment
• competitive salary
• “Elite” class health insurance (for employee and his/her children under 18)
• life insurance
• lunch allowance
• fitness allowance