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ICRA/SSU Administrator

Serbia, Remote Additional Locations: Romania, Remote;Hungary, Remote;Ukraine, Remote;Czechia, Remote 求人ID R0000030263 Category Clinical Trials
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About this Role

Parexel is currently seeking an experienced Study start up administrator to join us in Czechia, Romania, Serbia, Hungary and Ukraine, you be assigned to one of our key sponsors in the region.

Working as an Initiation CRA, you’ll be responsible for ensuring the completeness of Site Essential Document Packages as well as the Site Regulatory Packages. Reviewing essential documents, tracking and ensuring all files are in place in the eTMF.

Some specifics about this advertised role

  • Dedicated to one client.
  • Gathers all documents required for the purposes of enabling Site Initiation; includes the compilation of documents from multiple internal stakeholders and supporting functions to then distribute to the site in a structured and time sensitive manner.
  • Review investigator site essential documentation packages from CROs per process and sample as needed
  • May collaborate directly with sites regarding collection of documents and IRB timelines for site activation and ensure that relevant documents are uploaded into the eTMF.
  • May represent Site Start up on cross-functional study team (s) and/or sub-team(s); Attends Kick Off meetings to present SSU Roles and Responsibilities

Here are a few requirements specific to this advertised role.

  • 3 years in essential or regulatory document management in Pharmaceutical /CRO industry, understanding of clinical study start up requirements and working knowledge of relevant documentation. 
  • Strong familiarity with EUCTD/R and Federal Code of Regulations
  • Familiarity with Veeva Vault Clinical for CTMS and eTMF use
  • Excellent verbal and written influencing and training/mentoring skills, in local language and English   
  • Strong coordination and organizational skills  
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