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Accenture Pharmacovigilance Jobs 2026 | PV Services New Associate | B.Pharm BSc Nursing | 0-2 Years | Fresher

Accenture Pharmacovigilance Jobs 2026 | PV Services New Associate | B.Pharm BSc Nursing | 0-2 Years | Fresher

chandrakanth May 6, 2026
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🧬 Pharmacovigilance Services New Associate – Accenture 🧬

Accenture is hiring Pharmacovigilance Services New Associate for Pharmacovigilance & Drug Safety Surveillance. Excellent opportunity for freshers and candidates with 0-2 years experience.

πŸ“Œ Job Details

  • πŸ’Ό Skill Required: Pharmacovigilance Operations – Pharmacovigilance & Drug Safety Surveillance
  • πŸ‘¨β€πŸ’Ό Designation: Pharmacovigilance Services New Associate
  • πŸŽ“ Qualifications: Bachelor of Pharmacy / BSc Nursing
  • ⏱️ Years of Experience: 0 to 2 years
  • πŸ”„ Work Mode: Rotational shifts may be required

🏒 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 β€” 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. Visit us at www.accenture.com

πŸ“ What Would You Do?

  • πŸ“‹ Prioritise, book in, triage, and case processing activities for ICSRs in accordance with Client Guidelines, Regulatory due date, and TAT SLAs and KPIs
  • πŸ’» Perform end to end case processing as per agreed client requirement and case processing guidelines
  • πŸ“₯ Prioritize cases from Intake workflow, mails and other sources to create cases in global safety database
  • πŸ” Identify, review for validity of cases and move cases to respective workflow step based on case type
  • πŸ“Š Perform collection, evaluation, and submission of Adverse Event (AE) reports, transmission, and reconciliation of pharmacovigilance data
  • πŸ“ TMF (Trial Master File) review, download of AE reports from EVWEB and MHRA portal and importing AE reports on pharmacovigilance database
  • βœ… Review source documents for validity of ICSR, perform duplicate check and confirm medical significance
  • πŸ“§ Request missing minimum safety Information or clarification of erroneous data and send queries per Client SOP
  • 🏷️ Complete case processing including coding of medical history, suspect drug, adverse event and draft narrative into Global Safety Database
  • βš–οΈ Assess adverse events for seriousness, causality as per applicable Client SOPs, consulting medical reviewer when needed

βœ… What Are We Looking For?

  • πŸŽ“ Education: Bachelor’s Degree in Life Sciences
  • πŸ’» Technology Skills: Experience with MS Office, knowledge of safety database
  • 🧠 Medical Knowledge: Good knowledge of medical terminology including MedDRA and WHO-Drug preferred
  • ✍️ Writing Skills: Good medical writing skills
  • πŸ—£οΈ Communication: Good Communication Skills, Strong English proficiency (Reading, Writing, Listening, Speaking)

🎯 Key Performance Indicators

  • ⚑ Ability to learn quickly
  • 🀝 Consistent demonstration of company values/behaviors
  • ⏰ Adverse events evaluated accurately, cases processed within required timeframes to meet regulatory requirements
  • πŸ“ˆ Process cases with good quality metrics
  • πŸ“‹ Performs all work in accordance with regulatory, compliance and safety requirements

πŸ“‹ Roles and Responsibilities

  • 🏷️ Perform medical coding/Drug Coding for each ICSR using MedDRA and WHODD
  • πŸ“ Complete and review evaluation including reporter/company causality, prepare narrative and E2B sender’s comment field
  • πŸ’Š Processing all AEs, SAEs and SUSARs in Global Safety Database per company policies and SOPs
  • πŸ“‚ Drafting pharmacovigilance agendas and meeting minutes; accurately archiving PV documents
  • πŸ” Reviewing safety case data and other PV documents for completeness and accuracy
  • πŸ“€ Assisting with tracking, submitting and distributing reports
  • 🀝 Assisting liaisons with partners and cross-functional team members to ensure compliance
  • πŸ“Š Supporting ad-hoc deliverables or pharmacovigilance projects; participating in audits and inspections
  • βœ”οΈ Validate data consistency and make corrections as needed
  • πŸ”„ Determine if additional information is needed, obtain missing information as per Client SOP
  • βœ… Check for pending action items, follow-up, clarification, corrections and ensure resolution
  • πŸ“‘ Perform submissions in global safety database for AEs, SAEs and SUSAR cases, troubleshoot submission issues
  • 🌐 Perform translations of source document, case narrative, adverse events as applicable
  • πŸ“§ Monitoring, tracking and reconciliation of client mailboxes and other sources
  • πŸ”“ Perform paper and electronic unblinding process if required
  • πŸ“ Review responses to queries and add follow-up information to case narrative
  • ✏️ Review and perform case correction, case deletions as per SOPs within applicable timeline
  • πŸ—„οΈ Archive all communications/clarifications related to Case in Global Safety Database
  • ⬆️ Escalate issues outside normal scope to respective lead
  • πŸŽ“ Successfully complete and clear all applicable training within required timelines
  • πŸ”„ Open to get trained and moved across roles based on business requirement

🌟 Why Join Accenture

  • πŸ† Global leader in technology and operations services
  • πŸ“ˆ Exposure to international Pharmacovigilance & Drug Safety processes
  • 🌍 Work with clients across 120+ countries in 40+ industries
  • πŸ’» Training on Global Safety Database, MedDRA, WHODD, E2B
  • 🎯 Career growth in Life Sciences BPO and Clinical Research domain
  • 🀝 Strong focus on learning, innovation and employee development

πŸ“§ How to Apply

Apply Online

❓ FAQ

1) What qualification is required for Accenture PV Associate?

A: Bachelor of Pharmacy / BSc Nursing.

2) Is this role for freshers?

A: Yes, 0 to 2 years experience. Freshers can apply.

3) What skills are needed?

A: MS Office, medical terminology, MedDRA, WHODD knowledge preferred, English proficiency.

4) Is it work from home?

A: Not specified. Rotational shifts may be required.

5) What is the main responsibility?

A: ICSR case processing, medical coding, AE/SAE/SUSAR handling, PV data submission.

Great opportunity to start your career in Pharmacovigilance with Accenture!

Tags: Accenture Jobs, Pharmacovigilance Jobs, Drug Safety Jobs, PV Jobs, ICSR Jobs, MedDRA Jobs, WHO-Drug Jobs, B.Pharm Jobs, BSc Nursing Jobs, Fresher Jobs, Life Sciences Jobs, 2026

Post Views: 7

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