REF 1835123
24.06.2025 | Dubai | full time
General
Location: Dubai
Occupancy: full time
To join : immediately
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
Medical insurance provided
Publisher
direct employer
50 - 200 employees