Job Description
You live and breathe clinical trials – and want to apply your expertise where it truly matters? Welcome to Oviva.
Why Oviva?
At Oviva, our goal is a healthier future for all. We help people living with weight-related conditions access the most effective and accessible care.
We provide digital therapeutic programmes to support individuals dealing with obesity, high blood pressure, type 2 diabetes, prediabetes, and overweight. While weight loss is a primary goal for many of our users, our approach goes beyond the numbers on the scale – we focus on improving health, confidence, and quality of life.
Oviva is Europe's largest digital health provider in our field, and we're growing fast across the UK, Switzerland, Germany, and Poland. Join an organisation that has already supported nearly 1 million people – and continues to expand rapidly.
As Senior Clinical Trial Manager you will work closely with our Director of Clinical Trials. You will help translate regulatory and market access needs into robust study plans – and take full ownership of driving those studies through successful delivery.
You will play a key role in designing, executing, and evaluating our clinical trials, ensuring that we generate high-quality evidence that supports patient access and our regulatory strategy.
Your Responsibilities:
- Develop study protocols in collaboration with clinical, statistical, and regulatory teams
- Take full ownership of trial operations – from start-up to publication
- Coordinate external partners including CROs, trial sites, and technical vendors across Germany, Switzerland, and the UK
- Oversee budgets, timelines, milestones, and risk management
- Share your expertise to foster a collaborative, learning-oriented team culture
- Ensure data quality, regulatory compliance, and audit readiness at all times
- A degree in life sciences, medicine, or a related field
- Proven experience in protocol development, statistics, literature review, and clinical trial execution
- In-depth knowledge of ICH-GCP, ISO 14155, EU MDR, and local regulatory environments in DE, CH, and UK
- Hands-on experience with CTMS, EDC, eTMF, IWRS/eCOA, and user acceptance testing
- Strong communication skills, a problem-solving mindset, and collaborative spirit
- Fluent in English (spoken and written) - German is a plus!
- A meaningful role where your work drives real impact in healthcare
- A dynamic and purpose-driven environment in a fast-growing organisation
- Extensive training and development opportunities, including a personal learning budget
- Flexible working models and remote-first options to support your work-life balance
- A home office allowance to help you create your ideal workspace
- Competitive salary and company pension scheme
(a) = all: We mean everyone.
We believe in building a workplace where people genuinely want to be. We do this by putting our values at the heart of everything we do:
We put the patient first. We empower our teams. We make it happen.
Oviva is deeply committed to creating an inclusive culture – one that supports, celebrates, and amplifies the diverse voices of our team. We are a place where everyone can be their true self, and everyone is welcome.
We encourage applications from people of all backgrounds and identities, including (but not limited to) race, ethnicity, gender, sexual orientation, age, ability, religion, and socio-economic status. We actively seek candidates who bring unique perspectives to help us build a stronger, more inclusive team.
Oviva is a proud Disability Confident Employer, supporting all candidates and team members with disabilities.
Ready to make a difference? Join us in transforming digital healthcare – apply today!
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