Jobs in Opole, Poland
Discover more opportunities than anywhere else. Find more jobs nowBusiness Development Manager – Data & Cloud Market
Xebia
Specjalista ds. obsługi klienta - praca zdalna
ipracujzdalnie.pl
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Specjalista ds. obsługi klienta - praca zdalna
ipracujzdalnie.pl
Specjalista ds. obsługi klienta - praca zdalna
ipracujzdalnie.pl
Specjalista ds. obsługi klienta - praca zdalna
ipracujzdalnie.pl
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Wlgroup
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intent sp. z o.o.
Senior Clinical Trials Manager (a)
Job summary
A healthcare technology company in Poland is seeking a Clinical Trials Manager to take ownership of trial operations from start-up to publication. The successful candidate will coordinate with external partners and ensure compliance with regulatory standards. A degree in life sciences and experience in clinical trials are required. This role offers a competitive salary and flexible working models.
Benefits
Qualifications
- Proven experience in protocol development, statistics, literature review, and clinical trial execution.
- In-depth knowledge of ICH-GCP, ISO14155, EU MDR, and local regulatory environments in DE, CH, and the UK.
- Hands-on experience with CTMS, EDC, eTMF, IWRS/eCOA, and user acceptance testing.
Responsibilities
- Develop study protocols in collaboration with clinical, statistical, and regulatory teams.
- Coordinate external partners including CROs, trial sites, and technical vendors.
- Oversee budgets, timelines, milestones, and risk management.
Skills
Education
Tools
- 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, ISO14155, 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
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.