Pharmacovigilance Services Specialist

Accenture PLC; Bengaluru; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Accenture in Bengaluru is seeking a Pharmacovigilance Services Specialist with 7–11 years of pharmacovigilance experience to lead medical review tasks and ensure compliant case processing.

You will manage affiliate mailbox reconciliation, perform data entry, MedDRA coding, and submissions for ICSS per client guidelines, with rotational shifts as needed.

Qualifications

• Pharmacovigilance and drug safety surveillance exposure.
• Experience with case processing and MedDRA coding preferred.
• Understanding regulatory requirements for safety databases.

Responsibilities

• Manage the Affiliate Mailbox reconciliation and follow-up on serious and non-serious cases.
• Create and manage case identification, data entry, MedDRA coding, case processing, submission and follow-ups.
• Support rotational shifts as needed in a senior role.

Skills

Pharmacovigilance

Education

MBBS

Job description

Skill required:

Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation:

Pharmacovigilance Services Specialist

Qualifications:

MBBS

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?

• Looking for a Senior Medical Review Scientist
• 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 do analysis and solving of moderately complex problems.
• May create new solutions, leveraging and, where needed, adapting existing methods and procedures.
• The person would require understanding of the strategic direction set by senior management as it relates to team goals.
• Primary upward interaction is with direct supervisor.
• May interact with peers and or management levels at a client and or within Accenture.
• Guidance would be provided when determining methods and procedures on new assignments.
• Decisions made by you will often impact the team in which they reside.
• Individual would manage small teams and or work efforts (if in an individual contributor role) at a client or within Accenture.
• Please note that this role may require you to work in rotational shifts MBBS

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.