What You’ll Do:

• Collaborate with Solution Engineers and teams to gather and analyse study requirements for clinical trials of varying complexity.
• Produce functional documentation based on design inputs and ensure smooth integration with project timelines.
• Leverage all available tools to gather, assess, and document requirements using best practices.
• Manage and update system specifications throughout the project lifecycle, maintaining top-tier standards and validation processes.
• Identify risks, resolve conflicts, and ensure clear communication with all stakeholders to drive projects forward.
• Liaise with localization teams to develop translated versions of questionnaires (specific to Rater Station).
• Support SDLC validation and approval processes, while managing data extract and reporting requirements.

What You Bring:

• Bachelor’s degree or equivalent experience.
• Experience as a Business Analyst or in a similar role.
• Proven experience with the Software Development Life Cycle (SDLC) and technical documentation.
• A natural problem-solver with excellent analytical skills.
• Ability to gather and reconcile information from diverse sources and turn it into actionable insights.
• Strong communication and relationship-building skills, whether it’s presenting in meetings or crafting clear documentation.
• Proficiency with Microsoft Office applications (Word, Excel, Visio, PowerPoint).
• Ability to work independently with moderate guidance, as well as part of a global team.

Bonus Points If You Have:

• A background in software development or user interface design.
• Familiarity with GCP, 21 CFR Part 11, and/or SQL queries.