Senior Data Engineer, Clinical Data Management Services, R&D

Posted 4 Days Ago
Be an Early Applicant
3 Locations
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Leads development, administration, validation, and improvement of GxP-regulated clinical data systems and eClinical processes. Manages Medidata configurations, permissions, coding dictionaries, reporting, data outputs, and Spotfire visualizations. Provides expertise in CDISC standards, clinical trial data management, automation, AI-enabled tools, compliance, user training, and cross-functional collaboration across clinical development teams and vendors.
Summary Generated by Built In

Your role

Are you excited about developing and managing data and technology solutions that support the development of new medicines? We are looking for a Senior Data Engineer to play a key role in enabling data-driven clinical research and development through validated systems, high-quality data processes, and modern analytics solutions.

In this position, you will work closely with Clinical Operations, Data Management, Biostatistics, Statistical Programming, Quality, and external vendors to develop, integrate, and maintain GxP-regulated applications that support clinical trial execution, data reporting, visualization, and decision-making. Your expertise will help ensure that critical clinical systems and data solutions remain compliant, efficient, and fit for purpose throughout the clinical development lifecycle.

Responsibilities

  • Lead the development, standardization, and continuous improvement of eClinical processes and systems.
  • Manage system configuration, user access, roles, and permissions for Medidata applications.
  • Perform programming and reporting activities using software such as SAS, R, and Python.
  • Support computerized system validation activities in accordance with GxP and regulatory requirements.
  • Maintain MedDRA and WHODrug dictionaries, as well as synonym lists in Medidata Coder.
  • Develop customized reports and data outputs to support clinical development needs.
  • Serve as a subject matter expert for CDISC standards and related data structures.
  • Ensure deliverables and processes comply with SOPs, GxP, and applicable regulatory requirements.
  • Provide technical guidance, support, and training to Clinical system users and other stakeholders.
  • Drive process improvements, automation, and AI-enabled tools.
  • Plan and develop data visualizations for clinical studies using Spotfire.

This is a full-time position based in Espoo or Turku, Finland, or Cambridge, UK. Orion supports a hybrid working model, with employees working onsite three days per week and remotely for up to two days per week. This role reports to the Head of Clinical Development Data Services.

What you can expect from us

We offer an opportunity to work at the intersection of clinical research, technology, and data, contributing to solutions that support the development of new medicines. In this role, you will collaborate with multidisciplinary experts across Orion’s Clinical Development organization and play a key part in developing, improving, and maintaining the systems, processes, and analytics capabilities that enable high-quality clinical trial execution and data-driven decision-making.

At Orion, your work creates true impact and well-being for our customers, patients and society at large. ​ ​Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.

Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/.

What are we looking for?

  • Bachelor’s or Master’s degree, or an equivalent qualification, preferably in a scientific discipline such as Statistics, Computer Science, or Mathematics.
  • 7+ years of experience in the pharmaceutical industry and systems used in clinical development
  • Previous experience with Medidata applications, including Cloud administration, EDC, Coder, or Clinical Data Studio.
  • Advanced hands-on programming skills in SAS, R, or Python, along with strong data management capabilities. Knowledge of Spotfire is an advantage.
  • Strong understanding of clinical trial processes, GxP requirements, and industry best practices.
  • Interest in applying automation and AI-enabled solutions to improve programming efficiency and data quality
  • Strong attention to detail with excellent problem-solving, documentation, and cross-functional collaboration skills.

 

How to apply

Please submit your application, including CV, cover letter, and salary request by 20 September 2026. Please note that the applications are reviewed on a rolling basis throughout the application period. We kindly ask recruitment agencies and headhunters not to contact us regarding this vacancy.

For additional details contact Hanna Kivini, Head of Clinical Development Data Services, Tel. +358 50 966 7240 on Tuesday 8 September between 12pm-1pm EEST or Wednesday 16 September between 12.30pm-2pm EEST. 

Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person.

#LI-ORION

Your new team

Orion’s pharmaceutical innovations are created within its R&D organization. We employ over 400 top professionals in the field of drug discovery and development. We work globally: in Espoo and Turku in Finland, in Nottingham and Cambridge in the UK, and in Cambridge, MA, USA. Orion R&D and the Innovative Medicines business division are dedicated to making a transformation to become a global player in the pain and oncology therapy areas. 

About Us

Orion Pharma is a globally operating Nordic pharmaceutical company – a builder of well-being for over a hundred years.

We’re home to more than 4,000 Orionees around the world, and we’re proud to be known as a responsible employer and a great place to work. At Orion Pharma, people are truly valued and trusted, encouraged to grow, and supported by a culture where every voice is heard. We appreciate each other, strive for excellence, and build the future.

Together we develop, manufacture, and market human and veterinary pharmaceuticals and active pharmaceutical ingredients. Our extensive portfolio includes proprietary and generic medicines as well as consumer health products. The core therapy areas of our pharmaceutical R&D are oncology and pain. Proprietary products developed by Orion Pharma are used to treat cancer, neurological diseases, respiratory diseases, and more.

We offer careers with a clear purpose: empowering people to live their lives to the fullest.

About Orion

Skills Required

  • Bachelor's or Master's degree, or equivalent qualification, preferably in Statistics, Computer Science, Mathematics, or another scientific discipline
  • 7+ years of experience in the pharmaceutical industry and systems used in clinical development
  • Experience with Medidata applications, including Cloud administration, EDC, Coder, or Clinical Data Studio
  • Advanced hands-on programming skills in SAS, R, or Python
  • Strong data management capabilities
  • Strong understanding of clinical trial processes, GxP requirements, and industry best practices
  • Interest in applying automation and AI-enabled solutions to improve programming efficiency and data quality
  • Strong attention to detail, problem-solving, documentation, and cross-functional collaboration skills
  • Knowledge of Spotfire
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The Company

What We Do

Orion is a globally operating Nordic pharmaceutical company and builder of well-being. Rooted in Nordic values of trust and openness, the company focuses on developing treatments and conducting research to empower people to live their lives to the fullest. Operating in over 35 countries, Orion drives innovation in healthcare to improve health outcomes for millions of people worldwide.

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