Pharmacovigilance Services Specialist

Accenture in India; Bengaluru; On-site; INR 1,500,000 - 2,300,000; Full time

Job summary

Accenture in India seeks a Pharmacovigilance Services Specialist to lead pharmacovigilance operations, case processing, and data entry per client guidelines and global regulations. The role emphasizes MedDRA coding, adherence to safety workflows, and collaboration with senior management to meet team goals.

The position may involve rotational shifts and potential team contributions within a global PV framework, leveraging strong scientific and regulatory knowledge to ensure compliant case

Qualifications

• MBBS is required.
• 7–11 years of pharmacovigilance experience is expected.
• Experience with data entry, MedDRA coding and case processing.

Responsibilities

• Manage affiliate mailbox and reconciliation of reports.
• Perform MedDRA coding, case processing, submission and follow-ups.
• Handle ICSSRS safety database entries per regulatory guidelines.
• Analyse moderately complex PV safety data and problems.
• Interact with supervisor and peers for guidance on new tasks.
• May lead small teams or project efforts.
• Role may require rotating shifts.

Skills

Pharmacovigilance Operations - Pharmac

Education

MBBS

Job description

Skill required:

Pharmacovigilance Operations - 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 ICSSRS in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for?
• Primary skill - Pharmacovigilance & Drug Safety Surveillance - P3 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