Senior Clinical Science Manager
Oviva
Germany
Why Oviva?
At Oviva, we’re on a mission to make sustainable, personalized, clinically effective care accessible to everyone as we build Europe’s leading AI-powered chronic care platform. Our digital programmes help people manage weight-related illnesses by focusing on what matters most: improving health, building confidence, and enhancing quality of life.
To date, we have supported over one million people across the UK, Switzerland, and Germany. Our mission is powered by a dedicated team operating across four countries, including our hub in Poland. Every conversation, coaching session, and line of code brings us closer to a healthier future.
Our journey is accelerating: In 2026, we secured €200 million in Series D funding led by Kinnevik and a group of leading global investors. This investment fuels our next phase of growth, allowing us to scale our AI-enabled chronic care platform across Europe and expand our support to even more people living with chronic conditions.
Join us, and be part of the team making that future possible!
The Role:
To help bring our vision of accessible, evidence-based digital care to life, we’re seeking a Senior Clinical Science Manager to lead clinical research that directly improves patient outcomes.
You bring a scientific mindset with a hands-on approach. You’re proactive, precise, and passionate about pushing boundaries in digital health research. You are:
Experienced across the full clinical trial lifecycle (start-up through data interpretation).
Skilled in trial design, endpoint development, and data quality monitoring.
Familiar with ICH-GCP, ISO 14155, and EU MDR; prior experience with DiGA is a plus.
Collaborative, solution-focused, and thrive in cross-functional teams.
A fluent communicator in English (German is a bonus).
Essential:
MSc in Life Sciences, Medicine, Pharmacy, or Biomedical Engineering.
4–6 years of clinical research experience in pharma, biotech, or digital health.
As a Senior Clinical Science Manager, you will be at the heart of Oviva’s mission - designing and delivering clinical trials that fuel our regulatory submissions, patient access, and product evolution.
In this high-impact role, you will:
Independently lead protocol development with robust scientific rationale and operational feasibility.
Own study documents (protocols, CRFs, ICFs), ethics submissions, and regulatory compliance across the UK, Germany, and Switzerland.
Act as scientific lead during start-up, site management, and data interpretation phases.
Collaborate with CROs, KOLs, and advisory boards to ensure studies generate meaningful, regulatory-ready evidence.
Drive the production of Clinical Study Reports (CSRs), manuscripts, abstracts, and conference presentations to disseminate outcomes globally.
