Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation: Pharmacovigilance Services Specialist

Qualifications:MBBS/MD

Years of Experience:7 to 11 years

About Accenture

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What would you do

Responsible for Medical review of the aggregate and RMP report
Addresses all previous Health authority comments and adhoc requests received from Health authority.
Review and provide any noteworthy cases and published studies including pregnancy registries.
Discuss and provide medical analysis for all relevant sections of AR and RMP
To provide the conclusion regarding the current safety profile of the product.
Medical review of the aggregate and RMP report within agreed timeframes and to a high standard of accuracy. What are we looking for
Primary skill - Medical review of AR and RMP documents Roles and Responsibilities:
Participate in KOM, project planning, strategy meeting.
Providing inputs, insights from review of aggregated and RMPs
Perform QC of all the assigned aggregate reports and RMP documents
Addresses all previous Health authority comments and adhoc requests received from Health authority.
Review and provide any noteworthy cases and published studies including pregnancy registries.
Discuss and provide medical analysis for all relevant sections of AR and RMP
To provide the conclusion regarding the current safety profile of the product.
Address all medical queries, comments raised by the Client.
Perform QC of all the assigned aggregate reports and RMP documents.