Main Duties And Responsibilities
- * Develop and maintain Trial Participants database.
- Prepare a Trial Participants list from database refer to protocol inclusion\exclusion criteria.
- Communicate with Trial Participants to inform them about screening, and summarize them about study dates, Investigational medical product, study conditions.
- Communicate with Trial Participants to inform them about Screening results and the eligibility, and admission dates).
- Communicate with Trial Participants for ambulatory samples, repeat test, follow up adverse event, and follow up visit.
- Work on Clinical Management System (CMS) software to get Trial Participants information, and record Trial Participants arrival time during screening and study visits.
- Record the communication with Trial Participant in Trial participants communication details form.
- Work on platform system for data entry.
- Label blood and plasma tubes, and urine cups of the study.
- Give the compensation to trial participants and fills Trial participant Compensation Receipt Form
Job Requirements (Qualifications, Experience, Skills)* B.Sc. or diploma degree
* Communicator with a positive attitude towards work.
* Good knowledge of GCP and international guidelines.
* Good listening, interacting, flexible and dependable and communicating verbally and writing skills.
* Good command of Arabic and English languages both spoken and written.
* Very Good computer skills including windows, Microsoft Office (Excel, Word, PowerPoint, etc.)
