Senior Data Engineer, Clinical Data Systems (Hybrid)

Orion Corporation; Finland; Hybrid; EUR 90,000 - 120,000; Full time

Job summary

Orion Pharma, a Nordic pharmaceutical company, seeks a Senior Data Engineer in Clinical Data Management Services to drive data-enabled clinical development. Based in Espoo/Turku, Finland, or Cambridge, UK, you will work in a hybrid model to develop, validate, and maintain gxp-regulated data systems and analytics.

You will lead data standardization, Medidata configurations, and programming across SAS, R, Python, and CDISC data structures, delivering robust reports and visualizations for clinical

Qualifications

• Bachelor’s or Master’s degree in a scientific field with pharma experience.
• Advanced programming skills in SAS, R and Python.
• Experience with Medidata applications (EDC, Coder, CDS).
• Knowledge of CDISC standards and data structures.
• GxP and regulatory experience; SOPs compliance.

Responsibilities

• Lead development and improvement of eClinical processes and systems.
• Manage Medidata configuration, user access, roles and permissions.
• Program and report using SAS, R and Python.
• Support validation activities per GxP and regulations.
• Maintain MedDRA/WHODrug dictionaries and Medidata Coder.
• Develop customized reports for clinical development needs.
• Provide guidance and training to clinical system users.
• Drive automation and AI-enabled tooling.
• Develop data visualizations for studies using Spotfire.
• Ensure compliance with SOPs and regulatory requirements.

Skills

SAS programming

R programming

Python programming

Medidata

CDISC

Spotfire

Data visualization

GxP

Clinical data management

Education

Bachelor’s or Master’s degree in Statistics / Computer Science / Mathematics

Tools

Medidata Cloud administration

EDC (Medidata)

Medidata Coder

Clinical Data Studio

Job description

Orion Pharma, a Nordic pharmaceutical company, seeks a Senior Data Engineer in Clinical Data Management Services to drive data-enabled clinical development. Based in Espoo/Turku, Finland, or Cambridge, UK, you will work in a hybrid model to develop, validate, and maintain gxp-regulated data systems and analytics.

You will lead data standardization, Medidata configurations, and programming across SAS, R, Python, and CDISC data structures, delivering robust reports and visualizations for clinical