CRA

Responsibilitie********
- To ******** monitor an******** clinical trials in compliance withstudy protocol, GCP an********;
- To manage/resolve study relate******** at sites independently;
- To develop an******** goo******** effective communication withclinical research staff;
Requiremen********
- 1 years of experience or above on global Clinical trials is a must;
- University qualification in pharmacology/pharmacy, healthcare,me******** biotech or related;
- Demonstrate******** of, an******** ******** application of GCPan******** guidelines;
- Goo******** an******** ability both in English (skills at IELTS 6.5 orabove, or equivalent) an********;
- Excellent Communication skills;
- Love serving clients an********;
- Result-oriente******** can work under pressure;
- Goo******** player.