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Offer summary
(Summary generated by AI based on the full job description)
The project focuses on clinical trial data management at a growing CRO with foreign branches. Tools include EDC, Microsoft Excel and optionally R, SAS. Responsibilities include supporting the Clinical Data Manager, reviewing and cleaning EDC data, identifying discrepancies, maintaining documentation (including DMP and data review guidelines), supporting CRF development and testing, data reconciliation with vendors and preparing study status reports. The role offers remote work and employment at a company recognized as Top Employer 2026.
Clinical Data Coordinator II
Company: GRUPA NEUCA
from: 28 September 2026
to: 28 October 2026
salary not specifiedcontract of employment (full-time)
Offer parameters
level:mid
working mode:remote
location:Toruń, Kuyavia-Pomerania
Toruń, Kuyavia-Pomerania
Requirements
Your responsibilities
- support the Clinical Data Manager in the day-to-day management of clinical trial data,
- perform assigned data management activities in accordance with study-specific plans, procedures, SOPs, working instructions and applicable regulatory requirements,
- support the review and cleaning of clinical trial data entered in the EDC system in accordance with the study-specific requirements and agreed timelines,
- review data for completeness, consistency and accuracy and identify potential discrepancies requiring follow-up,
- assist in maintaining study documentation, including Data Management Plans (DMPs), data review guidelines, and other study-related documents,
- support the development, testing, and maintenance of Case Report Forms (CRFs) and electronic data capture (EDC) systems,
- contribute to the preparation of study metrics, data listings, and status reports,
- ensure data management activities are performed in compliance with applicable regulations, ICH-GCP guidelines, and company standards,
- support data transfer and reconciliation activities with internal departments and external vendors,
- participate in study meetings and provide updates on assigned data management tasks.
Our requirements
- degree or equivalent qualification in Life Sciences, Health Sciences, Pharmacy, Biotechnology, Data Management or a related discipline,
- previous experience in clinical research, clinical data management or a related field,
- knowledge of clinical trial processes and Good Clinical Practice (GCP),
- familiarity with Electronic Data Capture (EDC) systems and clinical data management processes,
- good working knowledge of Microsoft Office, particularly Excel,
- strong attention to detail and ability to work accurately with large volumes of data,
- good organizational and time-management skills,
- ability to work independently on assigned activities while operating effectively within a team,
- Good analytical and problem-solving skills,
- some programming skills (R, SAS) - nice to have.
What we offer
- work in a developing CRO in Poland with foreign branches,
- recommending appropriate solutions in projects,
- impact on changes in processes in the Data Management area,
- stable employment in the company awarded Top Employer 2026,
- work in an international team,
- remote work.
Clinical Data Coordinator II
I apply to:
GRUPA NEUCA
Toruń, Kuyavia-Pomerania
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