Walk in interview for Drug Safety Associate in Synowledge (Now a BIOCLINICA company)
Post: Drug Safety Associate
ESSENTIAL DUTIES AND RESPONSIBILITIES:
As Quality Check Reviewer
Review data entered in safety database for completeness and accuracy. Provide quality feedback to team resources
Track and maintain quality metrics
As Case Processor:
Responsible for data entry of individual case safety reports into the safety database.
Review and evaluate AE case information to determine required action based on and following internal policies and procedures
Process all incoming cases in order to meet timelines
Full data entry including medical coding and safety narrative
Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD).
Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
OTHER RESPONSIBILITIES:
Following up with sites regarding outstanding queries.
Follow up on reconciliation of discrepancies.
Follow departmental AE workflow procedures
Closure and deletion of cases
Mentor and guide the activities of the Dug Safety Associate.
Perform any other drug safety related activities as assigned
Perform literature review activities when trained and assigned.
Additional Information:
Experience : 1 + years
Qualification : BPharm / MPharm / BDS / Pharm D/BAMS/BHMS/BDS
Location : Mysore
Industry Type : Pharma / Biotech / Clinical Research
Functional Area : Drug Safety
Walk in Interviews
Friday, 22nd July 2016 Time : 10 AM to 4 PM
Saturday, 23rd July 2016 Time : 9 AM to 5 PM
Sunday, 24th July 2016 Time : 9 AM to 12 PM
VENUE:
Newbridge Business Centre Pvt. Ltd. B1/04-05, Ground Floor, B Wing, Boomerang Chandivali Road, Andheri (East), Mumbai 400072
Post: Drug Safety Associate
ESSENTIAL DUTIES AND RESPONSIBILITIES:
As Quality Check Reviewer
Review data entered in safety database for completeness and accuracy. Provide quality feedback to team resources
Track and maintain quality metrics
As Case Processor:
Responsible for data entry of individual case safety reports into the safety database.
Review and evaluate AE case information to determine required action based on and following internal policies and procedures
Process all incoming cases in order to meet timelines
Full data entry including medical coding and safety narrative
Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD).
Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
OTHER RESPONSIBILITIES:
Following up with sites regarding outstanding queries.
Follow up on reconciliation of discrepancies.
Follow departmental AE workflow procedures
Closure and deletion of cases
Mentor and guide the activities of the Dug Safety Associate.
Perform any other drug safety related activities as assigned
Perform literature review activities when trained and assigned.
Additional Information:
Experience : 1 + years
Qualification : BPharm / MPharm / BDS / Pharm D/BAMS/BHMS/BDS
Location : Mysore
Industry Type : Pharma / Biotech / Clinical Research
Functional Area : Drug Safety
Walk in Interviews
Friday, 22nd July 2016 Time : 10 AM to 4 PM
Saturday, 23rd July 2016 Time : 9 AM to 5 PM
Sunday, 24th July 2016 Time : 9 AM to 12 PM
VENUE:
Newbridge Business Centre Pvt. Ltd. B1/04-05, Ground Floor, B Wing, Boomerang Chandivali Road, Andheri (East), Mumbai 400072
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