Jobs in Bytom, Poland
STARSZY SPECJALISTA DS. ZARZĄDZANIA PROCESAMI
Poczta Polska S. A.
Discover more opportunities than anywhere else. Find more jobs nowSenior QA Engineer
Codest Ltd. Company No. 12590542, VAT number: GB363431020
Connect with headhunters to apply for similar jobsSenior Clinical Trials Manager (a)
Oviva
Business Development Manager – Data & Cloud Market
Xebia
Specjalista ds. obsługi klienta - praca zdalna
ipracujzdalnie.pl
Senior Data Engineer / Data Architect
Experis ManpowerGroup Sp. z o.o.
Senior Clinical Trials Manager (a)
Job summary
A health technology company in Poland is seeking a Clinical Trial Manager to lead the development of study protocols and coordinate trial operations. The ideal candidate should have a degree in life sciences and proven experience in clinical trial execution. This role allows for flexible working models and offers a competitive salary along with extensive training opportunities.
Benefits
Qualifications
- Proven experience in protocol development and clinical trial execution.
- In-depth knowledge of ICH-GCP and local regulatory environments.
- Hands-on experience with clinical trial management systems.
Responsibilities
- Develop study protocols in collaboration with various teams.
- Take ownership of trial operations from start-up to publication.
- Coordinate external partners including CROs and trial sites.
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.