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Data Analyst Avania Clinical

Vereniging In Beweging - Bilthoven - 30-07-2021 Naar vacature  


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Data Analyst

Avania is currently looking for a Data Analyst (full-time, 1.0 FTE), location Bilthoven office, The Netherlands.

Company Profile

Avania is specialized in and has over 30 years of experience in clinical investigations of medical devices, biologics and device-drug combinations. We organize patient studies across the globe and hold office in The Netherlands, USA and Australia. In the Analytical Services department, you will be working with a fast-growing team of approximately 30 Data Analysts and Biostatisticians that are mainly located in Boston and Bilthoven. At Avania, you’ll be working in a closely connected, involved and dynamic team that has a lot of expertise and experience, providing ample opportunity for both personal and career development.

Job Profile

As a Data Analyst (commonly referred to as Data Manager in CRO industry), you:
  • Review study protocol data management sections
  • Write Data Management Plans
  • Design Case Report Forms (data collection forms) based on the study protocol
  • Design and build databases for collection of study data
  • Specify and program data validation checks
  • Standardize data structures
  • Take care of database training for hospital staff
  • Review study data and work on cleaning the data
  • Identify data trends and safety concerns
  • Define and program data visualization dashboards (SAS, Power BI) and other trial data analytics
  • Take part in client communication and collaborate with other involved parties
  • Manage data analytics project deliverables and timelines
  • Will have an opportunity to contribute to cross functional work streams with statisticians and medical writers

Function requirements

  • Life sciences, Bio-informatics, Health Sciences, Human Movement Science, Computer Science, or other relevant master degree
  • Proficient in the use of computer and software systems
  • Experience with SAS, R, Power BI and/or any Clinical Database Management Software is a plus, not a requirement
  • GCP, ICH-E6, and/or ISO14155 knowledge is a plus, not a requirement
  • Accurate with strong attention to detail
  • Excellent communication skills
  • Team player with high energy and an ability to work independently or with a team
  • Stress resilient
  • Fluent in English 
  • Proficient in Dutch 
  • Permanently located in The Netherlands, preferably near the Bilthoven office
  • Preferably available for 0.8 to 1.0 fte

We offer

  • The possibility to be involved in all relevant aspects of a medical technology clinical investigation and work with project teams with staff from various disciplines
  • Well outlined training program for personal and career development
  • The opportunity to work in an international setting with colleagues located in Australia, Europe, and the United States
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