With offices in Berlin, Warsaw and Prague, KCR Placement is an international boutique provider of ‘fit for purpose’ resourcing solutions for a wide array of functions, including expert, managerial and senior executive ones. We specialize in finding the right talents for Pharmaceutical, Biotech, Medical Device companies and Contract Research Organizations across Europe. 

We're onboarding best-in-class candidates, so give us a chance to meet you!

Current Vacancy Highlights:




Clinical Data Associate / Estonia


Estonia, Office or home-based in Tallinn or Tartu



Opis Firmy

KCR Placement is a boutique provider of precisely tailored resourcing solutions. We specialize in high-speed and high-quality talent sourcing for the CRO, Biotechnology and Medical Device industries across Europe. Founded as a sister company of KCR, the KCR Placement team is supported by a specialized referral network of expert professionals and is dedicated to providing full-service recruitment services from job requisition to job offer. The company main services include Permanent Placement, Temporary Placement, Contract Placement, and Executive Placement. We also provide Labor Market Research and Reports. For more information please visit www.kcrplacement.com

KCR an international medium-sized CRO, is looking for a Clinical Data Associate. Your role will focus on clinical data review, query generation/resolution and reconciliation activities to support the delivery of clinical data according to client quality and project timelines.


Clinical Data Associate


The duties associated with the role include:

  • Performing data processing activities including data receipt, data entry and data review, using both manual and automated methods
  • Interacting with internal staff and Investigator sites as needed for discrepancy resolution
  • Encoding terminology entered into clinical database using MedDRA and other dictionaries and resolving encoding discrepancies
  • Coordinating collection and processing of laboratory data; including resolution of any inconsistencies or discrepancies
  • Supporting documentation maintenance and archiving procedures
  • The CDA may be required participate in teleconferences as required by the project, including those outside normal business hours

  • University degree or equivalent in Life Sciences area
  • Prior experience in clinical research, ideally within clinical data management field
  • Excellent command of English (both written and verbal)
  • Strong computer skills
  • Exceptional interpersonal skills coupled with an ability to work cross functionally in a globally diverse environment
  • Good understanding of ICH/GCP
We’re onboarding “best in class” candidates, so give us a chance to meet you!