Review and Assess all source documents and compile data in an adverse event report. Ensure completeness of documents, clinical safety data during data entry, tracking and interact with seniors in case of discrepancies.
Required Experience, Skills and Qualifications
Formal education
- Graduate, preferably in science
- Bachelor’s degree / Masters in Life sciences
- MBBS/BHMS/ BAMS/ BDS/ Paramedical degrees
- B. Pharm/ M. Pharm
- Bachelors / Masters in Clinical research
Job Type: Full-time
Salary: ₹150,000.00 to ₹175,000.00 /year
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