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
Our requirements
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 language proficiency
What we offer
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
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.
Oviva is a proud Disability Confident Employer, supporting all candidates and team members with disabilities.