Pharmacovigilance Services Senior Analyst | Bengaluru, India | Full-Time
Company Overview:
Accenture is a global professional services company with leading expertise in digital, cloud, and security solutions. With over 775,000 employees across 120+ countries, Accenture combines technology and human ingenuity to drive innovation, deliver value, and create positive change for clients, communities, and employees. The company fosters an inclusive, bias-free workplace with opportunities for professional growth, skill development, and global exposure.
Role Overview – Pharmacovigilance Services Senior Analyst:
Accenture is seeking an experienced Pharmacovigilance Services Senior Analyst to lead signal management activities and support safety surveillance within the Pharmacovigilance (PV) function. This role is responsible for authoring Signal Management Aid Review Team (SMART) reports, conducting literature reviews, managing Safety Surveillance Team (SST) meetings, and ensuring compliance with global regulatory and SOP requirements.
Key Responsibilities:
Conduct weekly literature reviews to identify potential safety signals for inclusion in aggregate reports.
Author and manage SMART reports using the Electronic Data Management System (B-EAMS), ensuring accuracy, timeliness, and compliance.
Schedule and host SMART and SST meetings, prepare slide decks, document action items, and distribute reports to stakeholders.
Liaise with Global Safety Officers (GSO) and PV Scientists to address potential safety signals.
Perform signal management activities per SOPs, guidelines, and job aids.
Archive supporting documents and maintain records in electronic repositories (SharePoint) as per timelines.
Provide timely responses to queries related to SMART reports.
Collaborate with IT systems (Tableau, BEAMS, SharePoint) where required.
Complete assigned training and maintain compliance with quality standards.
Qualifications & Experience:
Education: Bachelor of Ayurvedic Medicine and Surgery (BAMS), or a Bachelor/Master’s degree in Life Sciences.
Experience: 2–5 years in pharmacovigilance operations, with expertise in safety writing, aggregate reports, and signal management.
Knowledge of Good Pharmacovigilance Practices (GVP), ICH Good Clinical Practices, and clinical data management processes.
Strong written and verbal communication skills, with the ability to work independently and under tight timelines.
Experience in working effectively in international and multicultural environments.
Proficiency in MS Office products and familiarity with PV systems.
Skills & Competencies:
Attention to detail and high level of scientific accuracy.
Strong organizational skills with the ability to manage multiple projects.
Ability to plan, prioritize, and execute tasks efficiently.
Excellent interpersonal and professional communication skills.
Flexibility and adaptability to changing priorities and time zones.
Work Location & Schedule:
Bengaluru, India
Full-time role with potential coordination with US business hours as needed.
Why Join Accenture:
Work with a global leader in professional services driving transformative solutions across industries.
Exposure to cutting-edge pharmacovigilance processes and global PV operations.
Opportunities for professional growth, certifications, and international collaboration.
Inclusive, empowering workplace culture recognized globally as a World’s Best Workplace™.
Job Type: Full-Time
Experience Required: 2–5 years
For more information about Accenture, visit www.accenture.com.
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