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Senior Clinical Trials Manager (a)
Chełm
Nazwa pozycji
Senior Clinical Trials Manager (a)
Lokalizacja
Chełm
, Chełm, lubelskie, Polska
Firma
Oviva
Dodano
18. 9. 2025
Informacje o stanowisku
Senior Clinical Trials Manager (a)
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 is a plus!
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
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