Pharmacovigilance Services Associate

Accenture in India; Bengaluru; On-site; INR 400,000 - 700,000; Full time

Job summary

Accenture is seeking a Pharmacovigilance Services Associate in Bengaluru. The role involves managing drug safety case processing, MedDRA coding, and adverse event submissions in line with client guidelines and regulatory requirements.

The position may involve rotational shifts and requires 1–3 years of pharmacovigilance experience and a graduation qualification. The successful candidate will work within a team to ensure timely and accurate case handling, mailbox reconciliation, and escalation as

Qualifications

• Any Graduation.
• 1 to 3 years of experience in Pharmacovigilance/Drug Safety surveillance.
• Role may require rotational shifts.

Responsibilities

• Looking for a Drug Safety Associate.
• Manage affiliate mailbox reconciliation and follow-ups for Serious and Non-Serious cases.
• Create and manage case identification, data entry, MedDRA coding, case processing and submissions as per client guidelines.

Skills

Pharmacovigilance

Drug Safety

Case processing

Education

Graduation

Job description

Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications:Any Graduation
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?

• Looking for a Drug Safety Associate
• 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 ICERS 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