NEW
REF 1896559
8 hours ago | Abu Dhabi | full time
- General
- Location: Abu Dhabi
- Occupancy: full time
- Description
- Key Responsibilities:
Coordinate and oversee clinical trials in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
Screen, recruit, and enroll study participants; obtain informed consent and ensure compliance throughout the study.
Collect, process, and document study data accurately in case report forms and electronic data capture systems.
Schedule and manage study visits, procedures, and follow-up appointments.
Maintain regulatory documents, ethics submissions, and IRB approvals.
Liaise with sponsors, monitors, investigators, and internal teams to ensure protocol adherence and resolve study-related issues.
Report adverse events, deviations, and study progress to appropriate stakeholders.
Assist with budget tracking, inventory management, and study supplies.
- Requirements
- Experience: 1 year
- Bachelor degree
- Cv
- Provisions
- Salary: to be discussed
- Employment visa provided
- Transportation provided
- Housing provided
- Medical insurance provided
- Publisher
- MISPAH PIPELINE INSPECTION SERVICES L.L.C
- direct employer
- 51 - 200 employees