Pharmacovigilance Services New Associate

Accenture in India; Chennai District; On-site; INR 300,000 - 540,000; Full time

Job summary

Accenture is seeking a Pharmacovigilance Services New Associate in Chennai, India. The role focuses on product safety monitoring and case handling within a collaborative team.

You will perform data entry, MedDRA coding, case processing, and submissions in line with client guidelines and global regulatory requirements, with shift rotations possible. This entry-level role requires 0-1 year of experience and a degree in BSc/BDS/BPharm, offering exposure to international safety standards within a

Qualifications

• Bachelor degree in science or health field (e.g., BSc).
• Bachelor of Dental Surgery (BDS) or Bachelor of Pharmacy (BPharm).

Responsibilities

• Product safety monitoring and case handling.
• Data entry, MedDRA coding, case processing and submissions per guidelines.
• Work across shifts as required.

Skills

Pharmacovigilance

Drug Safety

Education

BSc

Bachelor of Dental Surgery

Bachelor of Pharmacy

Job description

Job Description

Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation

Pharmacovigilance Services New Associate

Qualifications

BSc/Bachelor of Dental Surgery/Bachelor of Pharmacy

Years of Experience

0 to 1 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?

• Product safety monitoring
• Product safety monitoring
• Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSSs 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 primary interaction is within your own team and your direct supervisor.
• In this role you will be given detailed instructions on all tasks.
• The decisions that you make impact your own work and are closely supervised.
• You will be an individual contributor as a part of a team with a predetermined, narrow scope of work.
• Please note that this role may require you to work in rotational shifts