
Clinical Research Study Coordinator
HomeNurse4U Pvt. LtdOriginal job description
Source: mustakbil.comEmployment type: Freelance / Contract (0.5 FTE; ~20 hrs/week; 4 hrs daily; travel time separate). On-site in Warszawa with some remote tasks.
Shift: Morning Shift
Location: Warszawa, Poland (on-site role; some remote activities)
Responsibilities:
- Clinical Trial Coordination (60%): coordinate on-site trial activities, manage participant visits and schedules, support hybrid visits.
- Clinical Trial Documentation (20%): maintain study records and trial documentation.
- Study Start-Up Support (10%): assist with site initiation and preparation activities.
- Site Training & Preparation (10%): support site training and readiness.
- Remote/Additional Tasks: pre-screening activities, appointment management, data entry, ongoing participant support, retention support, AE collection.
- Minimum experience: ~2 years as a Study Coordinator.
- Clinical research skills: clinical trial coordination, study start-up support, site training, clinical documentation, AE collection.
- Operational skills: participant scheduling, pre-screening, appointment management, data entry, supporting hybrid visits.
- Work mode: able to work on-site in Warszawa and perform some remote duties.
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