Oferta wygasa za:50 dni
Tryb pracyZdalna
Rodzaj umowyUmowa o pracę
Tryb rekrutacjiRekrutacja stacjonarna
Wymiar etatuPełny etat
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
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.
Benefity
Karta sportowa
Prywatna opieka medyczna
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