Pharmacovigilance Services Specialist

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation: Pharmacovigilance Services Specialist

Qualifications:MBBS/MD

Years of Experience:7 to 11 years

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world's largest network of Advanced Technology and Intelligent Operations centers. Our 784,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com

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.