(Poistunut julkaisusta)

Clinical Data Engineer
Bayer Oy

Alkuperäinen julkaisupäivä 29.1.2021

We are now looking for a professional with knowledge of clinical data structures and comprehensive software validation activities to work in a challenging global role based in a growing Data Science & Analytics (DS&A) team in Finland in Espoo as


CLINICAL DATA ENGINEER

 

Your tasks and responsibilities

  • Interpret protocol requirements to translate and document them into technical specifications
  • Develop study level programs for setup, conduct and closeout activities in the clinical data environments
  • Provision clinical study data to business consumers
  • Perform data loading/exchange activities ensure compliance against agreed data transfer specifications
  • Develop solutions based on gathered requirements from consumers to meet immediate and long-term needs of business customers
  • Monitor and maintain ongoing clinical study issues
  • Collaborate with functional representatives to ensure an understanding of the technical platforms for standardized solutions
  • Ensure adherence to program development, validation and maintenance principals to produce high quality data in line with Standard Operational Procedures (SOPs), for all data models/environments inclusive of supporting ways to define/enable automation and efficient re-usability
  • Ensure end-to-end data flow process where traceability requirements are met following Bayer standards
  • Complete all documentation associated with programming tasks (e.g. validation, report specifications etc.) in compliance with applicable SOPs
  • Estimate the time and resources needed to complete assignments. Track work progress and provide status reports to line manager and study team representatives.

 

Who you are

  • Bachelor/Masters with proven experience in a natural science, statistics, computer science or related field with experience in technical environment or equivalent, focusing on data warehousing and/or ETL activities
  • Knowledge of data warehousing principles, technologies and related ETL-processes
  • Experience with metadata repositories
  • Experience with a variety of programming languages including but not limited to PL/SQL, Java, SAS, C#
  • Proven hands-on experience programming in relational databases: SQL and Oracle PL/SQL Developer, TOAD or similar program development applications for realization of automations and programming activities in regulated environment
  • Knowledge of clinical data structures (i.e. CDISC standards for CDASH, SDTM and ADaM is an advantage or preferable)
  • Knowledge of comprehensive software validation activities using different methodologies (i.e. waterfall, agile etc.), inspections, analyses, and other verification tasks performed at each stage of the software development life cycle
  • Excellent oral and written communication skills in a global environment

We offer a competitive compensation, independent and challenging role in an international environment with a chance to develop your skills and experience further. To be considered for this exciting opportunity, please submit your application by Wednesday February 24, 2021. Candidates will be reviewed on continuous basis.

If you feel this unique role is just what you are looking for, we are keen to hear from you! For further information, please contact Luiz Giorgiani, Head of Clinical Data Management RED II, Data Sciences & Analytics, Monday February 8 at 14.00–15.00 (EET), phone +358 400 807868.

Functional area: Clinical Development & Operations
Seniority level: Professional
Location: This position can be filled in Espoo- Finland, Whippany -USA
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