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Clinical Trial Administrator Saint Petersburg Russia,  

PSI (company)


Posted on : 26 January 2017

Project Description


Clinical Trial Administrator
If you are keen to ensure high-level administrative assistantship to clinical project teams, be involved in document management and in-house quality control of multi-center international clinical trials of novel pharmaceuticals  you may be just the person we are looking for!


Responsibilities:
  • Communication point for hospitals participating in the clinical research projects for logistics & non-medical matters 
  • Communication with company departments and support services 
  • Work with big amount of documents, including their compiling, procurement, processing, translation and filing 
  • Maintaining project team working files, project-specific tracking systems, calendars and schedules 
  • Preparation of draft agendas and minutes of project review meetings, organization and assistance at project-specific meetings 
  • Technical assistance during internal and third-party study audits 
  • Receiving and routing mails and incoming calls 
  • Daily proactive support to clinical research teams with miscellaneous clerical duties 


Qualifications
  • University Degree 
  • Administrative work experience, preferably in an international setting 
  • Advanced English (spoken and written) 
  • Good organizational and planning skills 
  • Detail-oriented, able to multi-task and work effectively in a fast-paced environment 
  • Good problem solving abilities, flexibility 
  • Team oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects 
  • Proficient user of standard MS Office applications (Word, Excel and PowerPoint) 
 

Offer:
  • We provide high-quality employment, competitive salary, and a positive friendly work environment. 
  • It is a great chance to join the company that really cares for its people, and invests in their professional development and success!

Locations

RUSSIA ST. PETERSBURG

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