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2017-43356

2017-43356

Title 
Data Coordinator- Part time (Barcelona)
Job Locations 
-
Spain-Barcelona
Posted Date 
10/9/2017

More information about this job

Overview

As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

 

At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

 

At PRA, borders do not create boundaries. PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.

Responsibilities

We are looking for a Study Coordinator/ Data Coordinator based in Barcelona to support the preparation and conduct of studies by reviewing study data, receiving and tracking study documents and entering data into clinical databases and Case Report Forms (CRFs) and provide support during monitoring visits as well as archiving clinc study documents.

 

  • Work actively in project team environment
  • Oversee the document flow to ensure process is being followed for each study
  • Assist with clinic study set-up activities as needed
  • Assist with source document QC as needed
  • May ensure CRFs and/or electronic CRF database is available prior to the study
  • May participate in the creation and review of CRF/eCRF database
  • May ensure source documents are delivered to the clinic prior to study check in
  • May ensures source documents are QC’ed prior to data-entry
  • Transcribes information from the source documents to CRFs as outlined in the instructions and within specified timelines
  • Assists with query resolution if needed
  • Ensures all filing for studies is complete and according to filing instructions
  • For paper studies ensure that CRFs/DCFs are in order at the end of the study
  • Assists with archiving tasks as needed

Qualifications

  • Has knowledge of the drug development process. 1 year of experience in a similar role preferred.
  • Effectively demonstrates oral and written communication skills Basic knowledge of medical terminology Competent with Excel, Microsoft Office Suite and data processing Knowledge of ICH, GCP and good documentation practices in clinical research
  • High School Diploma, G.E.D., or secondary vocational education required
  • Fluent in English and Spanish

 

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