What You'll Do
Support the execution of clinical trials by managing essential documentation, including study protocols, case report forms, and entries in Electronic Data Capture (EDC) systems. Assist with identifying and enrolling eligible patients, ensuring informed consent and privacy requirements are properly documented. Coordinate logistics in alignment with study timelines and procedures.
Perform accurate data entry, conduct quality reviews, and resolve queries to maintain high data integrity. Engage in patient education to support understanding of trial processes. Serve as a point of contact for study monitors and respond to operational inquiries. Handle routine administrative duties essential to smooth trial operations.
Requirements
- Hold a bachelor’s degree in life sciences or have equivalent education and experience in a clinical or medical environment
- Demonstrate familiarity with clinical trial workflows, protocols, consent forms, and study schedules
- Possess strong knowledge of medical terminology
- Be proficient in MS Office applications, including Outlook, Word, Excel, and Access
- Have 1–2 years of experience as a Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator at a trial site
- Be fluent in Polish and able to communicate effectively in English
Technical Stack
Electronic Data Capture (EDC) systems, MS Office (Outlook, Word, Excel, Access)
Benefits
- Part-time schedule of 24 hours per week
- Option to work remotely one day per week
- Supportive and inclusive work environment
- Engagement in projects with measurable impact on healthcare
- Collaboration within a global research network
- Health and wellness benefits
- Eligibility for incentive plans, bonuses, or additional compensation
