Pharmacovigilance Services Associate

Accenture; Chennai District; On-site; INR 450,000 - 600,000; Full time

Job summary

Accenture in Chennai is seeking a Pharmacovigilance Services Associate to join our safety surveillance team. You will be responsible for intake, review and processing of adverse event reports in line with global regulations and client guidelines.

The role requires a Bachelor or Master of Pharmacy and 1–3 years of experience, with the ability to work in shifts as needed. You will contribute to data entry, MedDRA coding and case processing for ICSS in our safety database.

Qualifications

• Bachelor of Pharmacy or Master of Pharmacy required.
• 1–3 years of experience in pharmacovigilance or drug safety surveillance preferred.
• Experience with safety reporting regulations and MedDRA coding is a plus.

Responsibilities

• Handle Individual Case Safety Reports processing.
• Oversee intake, review, assessment and processing of adverse event reports for timely safety reporting.
• Manage Affiliate Mailbox reconciliation and all follow-ups for Serious and Non-serious cases.
• Create and manage case identification, data entry, MedDRA coding, and submission per client guidelines.

Skills

Pharmacovigilance & Drug Safety

Education

B.Pharm / M.Pharm

Job description

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation: Pharmacovigilance Services Associate

Qualifications:Bachelor of Pharmacy/Master of Pharmacy

Years of Experience:1 to 3 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?

• Individual Case Safety Report Processing
• Responsible for the intake, review, assessment, and processing of adverse event reports to ensure accurate and timely safety reporting in compliance with global pharmacovigilance regulations and company quality standards.
• Management of the Affiliate Mailbox reconciliation of reports per process and performance of all written follow up attempts to include both Serious and Non serious cases
• Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSS in the safety database as per client guidelines and applicable global regulatory requirements.

What are we looking for?

• Primary skill - Pharmacovigilance & Drug Safety Surveillance - P1

Roles and Responsibilities:

• In this role you are required to solve routine problems, largely through precedent and referral to general guidelines.
• Your expected interactions are within your own team and direct supervisor.
• You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments.
• The decisions that you make would impact your own work.
• You will be an individual contributor as a part of a team, with a predetermined, focused scope of work.
• Please note that this role may require you to work in rotational shifts Bachelor of Pharmacy,Master of Pharmacy

Equal Employment Opportunity Statement

All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.

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