REF 1510178
18.04.2024 | Dubai | full time
General
Location: Dubai
Occupancy: full time
Description
Instructs research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures. Collaborates with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
Requirements
Bachelors degree in a health care or other scientific discipline or educational equivalent,
At least 2 years of CRA experience of on-site monitoring visits,
Requires frequent travel to sites
Excellent command of Arabic and English language
Provisions
Salary: to be discussed
Employment visa
Publisher
direct employer
more than 200 employees