
Analyst_(of Clinical Research Organization)
24 hours ago
Role & responsibilities
- Should perform sample processing smoothly as well as project execution with in assign time.
- Should handle instrument as well as QA observation.
- Should coordinate with Group members/ Group leader/ Lab manager
- Should be able to inspect raw data as per defined procedure.
- Should report inspection result properly.
- Should verify calibration record.
- Should maintain GLP in Lab.
Preferred candidate profile
- 3-5 Years of Experience in Clinical Research Organizations only (Bio-Analytical Department)
- Qualification: MSC
- Immediate to 20 days joiners are preferred.
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