NEW
REF 1798288
35 hours ago | Abu Dhabi | full time
- General
- Location: Abu Dhabi
- Occupancy: full time
- Description
- Coordinated multiple clinical trials, managing participant recruitment, informed consent processes, and ensuring protocol adherence.
Monitored patient data and recorded adverse events, ensuring accuracy and compliance with Good Clinical Practice (GCP) guidelines.
Collaborated with principal investigators, sponsors, and regulatory authorities to maintain study integrity and streamline workflows.
Prepared regulatory documents and assisted in Institutional Review Board (IRB) submissions, maintaining thorough documentation for audits.
- Requirements
- Experience: 1 year
- Secondary certificate
- CV
- Provisions
- Salary: to be discussed
- Publisher
- direct employer
- 51 - 200 employees