Jobs in Kielce, Poland
STARSZY SPECJALISTA DS. ZARZĄDZANIA PROCESAMI
Poczta Polska S. A.
Junior Salesforce Developer - program szkoleniowy
Britenet
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Britenet
Doradca Techniczno- Handlowy (branża grzewcza)
Business Bridge Group Sp. z o.o.
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NMS KORPO
Asystent / ka Menadżera realizacji inwestycji
EkoEnergia Polska
Specjalista ds. Administracji Personalnej i Płac
EkoEnergia Polska
Specjalista ds obsługi klienta (j. francuski)
Barlinek SA
Senior Clinical Trials Manager (a)
Job summary
A healthcare organization is seeking a dedicated Clinical Operations Specialist to develop and manage clinical trial protocols. You will coordinate with various teams, ensure compliance, and oversee trial operations from start to finish. The ideal candidate holds a degree in life sciences and possesses strong experience in clinical trial execution. The position offers flexible working options, extensive training, and a competitive salary.
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.
- Hands-on experience with clinical trial management systems and related tools.
Responsibilities
- Develop study protocols in collaboration with clinical, statistical, and regulatory teams.
- Take full ownership of trial operations from start-up to publication.
- 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.