Pharmacovigilance Services Assoc Manager

Accenture in India; Chennai; On-site; INR 1,800,000 - 2,500,000; Full time

Job summary

Accenture in India is seeking a Pharmacovigilance Services Associate Manager with MBBS and 10–14 years of experience to lead medical review of ICSRs and ensure timely, compliant case processing. You will oversee MedDRA coding, causality assessment and data integrity in the Global Safety Database, while guiding a cross-functional PV team across client projects.

Responsibilities include prioritizing medical reviews per SLAs, reviewing source documents and providing client-ready causality comments,

Responsibilities

• Prioritize medical review for ICSRs per Client Guidelines, regulatory due dates, TAT SLAs and KPIs.
• Verify and confirm adverse events, MedDRA coding, seriousness, labeling, causality and provide a company causality comment per SOP.
• Create and manage case identification, data entry, MedDRA coding, case processing, submission and follow-ups.
• Review source documents to ensure medical accuracy and correct database entry.
• Lead training of internal and cross-functional PV team members on processes.
• Coordinate case routing and medical assessment questions with the client and triage associates.

Job description

Job Description

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation: Pharmacovigilance Services Assoc Manager

Qualifications: MBBS

Years of Experience: 10 to 14 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?

• Prioritize medical review for Individual case safety report (ICSRs) in accordance with Client Guidelines, Regulatory due date and turn around me (TAT) service level agreement (SLAs) and key performance indicator (KPIs).
• Verify and confirm on the selection of adverse events, appropriate MedDRA coding, seriousness, labeling, causality of adverse events and provide a company causality comment as per client SOP
• Prioritize medical review for Individual case safety report (ICSRs) in accordance with Client Guidelines, Regulatory due date and turn around me (TAT) service level agreement (SLAs) and key performance indicator (KPIs).
• Verify and confirm on the selection of adverse events, appropriate MedDRA coding, seriousness, labeling, causality of adverse events and provide a company causality comment as per client SOP
• Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for IC... (truncated for brevity)
• Prioritize medical review for Individual case safety report (ICSRs) in accordance with Client Guidelines, Regulatory due date and turn around me (TAT) service level agreement (SLAs) and key performance indicator (KPIs).
• Verify and confirm on the selection of adverse events, appropriate MedDRA coding, seriousness, labeling, causality of adverse events & provide a company causality comment as per client SOP.
• Review the source documents and narrative to assure medical accuracy pertaining to the case is appropriate and entered Global Safety Database.
• Write company causality comment Roles and Responsibilities:
• Prioritize medical review for Individual case safety report (ICSRs) in accordance with Client Guidelines, Regulatory due date and turn around me (TAT) service level agreement (SLAs) and key performance indicator (KPIs).
• Verify and confirm on the selection of adverse events, appropriate MedDRA coding, seriousness, labeling, causality of adverse events and provide a company causality comment as per client SOP.
• Review the source documents and narrative to assure medical accuracy pertaining to the case is appropriate and entered Global Safety Database.
• Write company causality comment and route the case to applicable workflow as per Client SOPs
• Constantly update domain and operations skills as per the changing client requirements by reading the updated version of SOPs
• Lead the training of internal and cross-functional team members.
• Actively involved in case discussion with client and provide the valuable inputs to the team.
• Confirm and advise on the medical assessment queries from case processing associate, literature reviewers, quality reviewers and triage associates.
• Validate data consistency and update the relevant database fields for any changes as needed in accordance with Client SOPs