Clinical Data & Device Specialist

All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way.

The Role

We are hiring a Clinical Data & Device Specialist to support Sava’s clinical operations projects. You will play a central role in data and device management activities through trial set up, conduct, and lock, working with cross‑functional stakeholders to ensure seamless collaboration in clinical studies, with a strong focus on data quality, device management and system design. You’ll work cross‑functionally with Clinical Affairs, Quality Affairs & Regulatory, Technical teams, and study partners to support high‑quality clinical trial execution across data, device, and study systems. You’ll manage clinical data activities from start‑up through database lock, support investigational device shipment, tracking, inventory, and accountability, and help ensure full traceability between sites and sponsor. This is a hands‑on, high‑ownership role focused on maintaining data integrity, strengthening compliance across EDC, eTMF, and study documentation, and building scalable processes that improve how Sava runs increasingly complex clinical studies.

What You’ll Do

• Conduct clinical data management activities from start‑up to lock, including data collection, validation, cleaning, medical coding, EDC checks, and reconciliation processes to ensure data integrity.
• Own investigational device management across studies, including coordinating shipments, tracking, inventory, and accountability to ensure compliance and full traceability between sites and sponsor.
• Lead the design, development, and review of Case Report Forms, Data Management, Validation and Data Review Plans and other study set‑up activities to maintain quality control and accurate data.
• Monitor real‑time data and document management across EDC, eTMF, and study systems to maintain compliance. Proactively identify trends, protocol deviations, and data quality risks.
• Identify and implement better processes across data flow, operations, device and document management. Not just run studies, but improve how they’re run.
• Work cross‑functionally with Clinical Affairs, Quality Affairs & Regulatory, and Technical teams to improve device traceability and data management processes across the study lifecycle.

What We’re Looking For

• 3 to 4+ years of experience in clinical operations, ideally within medical devices.
• Technical background such as biomedical engineering, maths, or life sciences.
• Hands‑on experience with managing EDCs, eTMFs, and coordinating clinical data, device, and document workflows.
• Strong operational instinct; you spot gaps and risks before they surface in a report.
• Highly organised with genuine attention to detail, not just as a line on a CV.
• Comfortable in fast‑moving, ambiguous environments where the process doesn’t always exist yet.
• Clear communicator with a bias for action and solution‑oriented thinking.
• Motivated to build and improve systems, not just execute them.
• Solid understanding of ISO 14155, ICH GCP, and local regulatory requirements such as MHRA or FDA.

Bonus Points For

• Experience with medical device clinical studies, particularly in sensor or wearable technology, diabetes trials, or CGM.
• Experience working in regulated environments, medical devices preferred.

Why Sava

This is a high‑ownership, high‑responsibility role in a company that is building something complex, meaningful, and fast. The expectations are high, the learning curve is steep, and the work is often messy – but the impact is real. We don’t have room for egos or passengers. What we do have is a team of thoughtful, driven, and mission‑aligned people who are committed to building something better and doing it with urgency and integrity.