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The Senior IT Engineer – R&D acts as the interface between the R&D business units and the Global IT organization. This role is responsible for capturing, assessing, prioritizing, and managing business demands related to digital and IT solutions. The ideal candidate will ensure alignment between R&D strategies and IT capabilities, fostering innovation and driving value through technology.
Job Responsibility:
Collect and analyze business requirements from R&D stakeholders
Translate business needs into functional and technical specifications
Collaborate with IT teams (architecture, development, support) to evaluate feasibility and define solution proposals for R&D use cases
Support the management of software implementations and data migration projects for the R&D solutions’ portfolio
Support the prioritization of initiatives based on business value, urgency, and alignment with strategic objectives
Contribute to the evaluation and development/implementation of AI initiatives for R&D use cases
Monitor the demand pipeline and maintain a clear overview of ongoing and planned IT R&D initiatives
Facilitate workshops and meetings between business and IT to ensure shared understanding and alignment
Contribute to building business cases for new IT R&D initiatives
Support change management activities and user adoption of delivered solutions
Ensure compliance with IT governance, data privacy, and security standards
Act as a key point of contact for R&D departments regarding IT topics
Requirements:
Bachelor's or Master’s Degree in Information Technology, Statistics, Biotechnology or other relevant field
4–6 years of experience in IT in the Life Sciences/Biotech/Pharma sector
Solid understanding of IT R&D processes and/or application management with a proven track record of delivering results across multiple project settings
Strong understanding of the R&D Pharma environment and experience in one or multiple areas such as e.g. Clinical, Pharmacovigilance, Regulatory, Medical Affairs
Knowledge of R&D software such as electronic Trial Master Files, Clinical Data Management solutions, Pharmacovigilance and Regulatory applications
Experience with GxP and GAMP5 frameworks
Proven experience in managing vendor relationships
Familiarity with Agile, Scrum, and/or Waterfall methodologies and ideally Project Management tools (e.g. SmartSheet, Microsoft Project)
Proficiency in Microsoft Office Suite
Strong communication and stakeholder management skills
Analytical mindset and problem-solving capabilities
Ability to work independently and handle multiple demands simultaneously
Ability to plan projects, work under deadlines and prioritize according to evolving business requirements
Team player with a proactive and business-oriented attitude
Demonstrable ability to think strategically and creatively while applying sound business judgment and quantitative analytics
English language proficiency
Nice to have:
Knowledge of the Veeva software portfolio is a plus
Understanding of Computer System Validation processes is a plus
What we offer:
competitive salary
comprehensive benefits
extensive opportunities for professional growth and development
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