REF 1883275
30.08.2025 | Abu Dhabi | full time
- General
- Location: Abu Dhabi
- Occupancy: full time
- Description
- During study visits, they assist participants, collect data, and ensure that all procedures are performed correctly and safely. In the event of adverse events or unexpected occurrences during the trial, clinical research coordinators are responsible for managing and reporting these incidents.
- Requirements
- Associate degree in nursing or related field.
2+ years in healthcare.
Analytical mindset.
Attention to detail.
Exceptional interpersonal skills.
Outstanding written and verbal communication.
Excellent organizational skills.
- Provisions
- Salary: to be discussed
- Residence visa provided
- Transportation
- Publisher
- direct employer
- up to 50 employees