ÓÐÐËȤ×öÁÙ´²Ñо¿µÄÁªÏµÎÒ £¨TTSH RA position openings£©please send me your CV if you are interested!
RA1
You will provide assistance to the investigators in the conduct and implementation of clinical research according to good clinical practice guideline.
You will co-ordinate all activities related to the studies including preparing study protocols, IRB application, study site start-up, screening and recruitment, consent taking, retrieval of data from medical records, data entry, perform phlebotomy, schedule subjects for follow-up visit and ensure compliance with study protocols.
You will also help in any other duties as assigned by the supervisor and investigators.
RA1
Requirement
1. Bachelor¡¯s Degree in Nursing or Science; or a Diploma in Nursing or Science with at least 2 years¡¯ relevant local work experience in related field
2. Ability to work both independently and in a team
3. Ability to perform pblebotomy
4. Proficient in MS office applications
5. Good communication and interaction s (more...)
How to contact with you?