To perform triage, duplicate check, book in and data entry in the safety database received from all type of reports Tracking and regularly following up of various ICSRs.
To perform the thorough quality review of cases.
To submit the cases to various regulatory authorities. Screening of the global literature review.
Social media screening.
Qualification & Experience
B.Pharm / M.Pharm
Minimum experience 1 to 2 years for junior & 3 to 4 years of senior