Cipla Ltd recruitment 2018-Apply online
Job Description
1. JOB PURPOSE
Support PV reporting activities case processing, literature reporting
2- Major Activities / Tasks
To ensure that regulatory reports are approved and submitted to partners or regulatory authority in appropriate format and within the appropriate timelines.
To ensure that source documents pertaining to regulatory authoritys acknowledgement of ICSRs are archived in Argus.
To process and review cases processed by the case processors for quality, MedDRA coding, narrative, and overall consistency with source documents, SOPs.
To maintain quality tracker of reviewed cases.
To provide periodic quality improvement feedback to case processors.
To act as subject matter expert while developing/updating SOPs case processing.
To identify areas of improvement in terms of compliance, quality, and productivity
To escalate instances of repeated case processing errors and non-compliance.
3. MAJOR CHALLENGES
Timely case processing and QC activities
Educational qualifications:
B Pharm or M Pharm
Relevant experience:
01 years of pharmacovigilance ICSR experience
Post Name : Trainee-drug Safety Department
Educational Qualification :UG:B.Pharma – Pharmacy PG:M.Pharma – Pharmacy, Post Graduation Not Required-0 -1 yrs
Location :India-Mumbai
Cipla Ltd recruitment 2018-Apply online
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