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R and D Clinical Scientist (27809) - Belgium   We are Urgently looking for a R and D Clinical Scientist

BrightOwl managed [?] Project on hold
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Project Types : Permanent position ,
FTE : 100 %
Min.Experience : 3 year
Start Date : ASAP
End Date : N/A
Posted on : 12 July 2017

Project is currently here

Step 1
Step 2
BrightOwl Screening
Step 3
BrightOwl Interview
Step 4
Company Screening
Step 5
Company Interview
Step 6
Budgets & Contracts
Step 7
Position filled

Project Description

Main accountabilities:

  • Acquire in-depth understanding of available patient-level datasets provided through the platform solutions and creating real world data insights
  • Formalize inclusion/exclusion criteria from clinical trial protocols into queries providing relevant and accurate results as input for clinical research management decisions
  • Analyze results, generate reports and present outcomes to clinical research teams within the company
  • Provide input on user requirements for trial design, feasibility analysis, site selection and Electronic Patient Chart Review and support the development of a metrics framework
  • Develop test plans and test against set criteria for evaluating the performance and usability of the platforms
  • For the platforms used: Evaluate and measure data quality, software functionality and analytic tools and provide constructive feed-back to all stakeholders
  • Pro-actively continue to strengthen subject matter expertise on query formalization and data mapping and quality of source data from healthcare providers with a good understanding of the hospitals, service provider and clinical research teams positions, especially also leveraging on knowledge about the healthcare settings in different geographies (North America, EMEA and Asia) for correct interpretation on clinical research insights


Project FTE 100%
Work from home:   Not Allowed
No. of Positions:   1


Analytical thinking Adaptability Collaboration Communicative Coordination Dependability Efficiency Flexibility Independence Interest in knowledge Innovative thinking Organization Proactivity Perspective Striving Strategic thinking


medical sciences Clinical research Healthcare Healthcare industry clinical data coding Clinical trials OMOP

Skills and Expertise

Analytical skills Analyze data Interpret data Advise on medical perspectives Administrative support Analyze data/information to determine potential relationships. Analyse growth / improvement potential EHR EMR Monitor data diplomatic team player SQL Interact with CROs


medical sciences


Professional Proficiency
Good to have
Professional Proficiency
Good to have

Desired Skills & Experience

Expected experiences, technical & personal skills:

  • Prior experience working with patient data, including clinical data warehousing, clinical information systems, EMR, drug/disease claims information
  • Strong skills in working with clinical data coding systems (ICD9/10, LOINC, SNOMED, ATC), anatomic pathology, and clinical standards
  • Extensive knowledge of clinical trial processes, protocol design, definition of eligibility criteria and study placement
  • Familiarity with commercial or non-commercial EHR and patient level data repositories and experience with computer-based search tools, data analytics for structured and unstructured medical data (text mining)
  • Knowledge and understanding of the EU and US health care environment and data privacy is an asset
  • Capable to help monitor the quality control and experienced with analysis of large biomedical data sets for clinical research
  • Outstanding analytical skills and proficiency in using analytical tools
  • Diplomatic team player with excellent presentation and reporting skills
  • Solution-oriented

Required qualifications:

  • University degree in medical sciences, with a strong affinity for medical informatics
  • At least 3 years of experience in a clinical research environment in a CRO, the pharmaceutical industry or in a hospital clinical (research) setting
  • IT proficiencies: Intermediary or advanced knowledge about SQL, excel, clinical research data mapping and data profiling; knowledge about OMOP is an asset
  • Fluency in English, any other language is a key asset in a European context