Clinical Research Associate I or II (Poland)
Alimentiv(4 months ago)
About this role
A training-focused Clinical Research Associate (CRA) role based in Warsaw that supports and observes clinical site monitoring services both remotely and onsite. The position provides exposure and training across clinical site monitoring, ensuring protocol, SOP, and regulatory (ICH GCP) compliance while supporting site management and patient recruitment activities. The role maintains collaborative relationships with stakeholders and supports study activities including remote data review, RBM, and TMF/document oversight.
Required Skills
- Site Management
- Remote Monitoring
- Onsite Monitoring
- Data Review
- Query Resolution
- Risk Based Monitoring
- Regulatory Compliance
- GCP
- TMF Management
- Stakeholder Relations
+5 more
Qualifications
- College Diploma or Degree
- SoCRA
- CCRA
- ACRP
About Alimentiv
alimentiv.comAlimentiv is a gastrointestinal-focused clinical research organization (CRO) that accelerates GI clinical trials through a specialized site network and integrated trial services. They provide end-to-end support including site operations, medical imaging, and biomarker discovery to help sponsors design, conduct, and analyze GI studies. Alimentiv positions itself as a partner for biotech and pharma teams needing disease-area expertise and integrated diagnostics to improve trial efficiency and decision-making.
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