PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

Accenture Pharmacovigilance & Clinical Data roles

Published on

Accenture is actively hiring across multiple roles in Pharmacovigilance, Clinical Data Management, and Quality Assurance in India. These opportunities are ideal for B.Pharm, M.Pharm, MBBS, and life sciences graduates with 1โ€“14 years of experience looking to build or advance their careers in drug safety and clinical research.

With positions open in Bengaluru and Mumbai, this hiring drive spans entry-level to managerial roles, making it one of the most comprehensive life sciences recruitment drives currently open.

Advertisement

๐Ÿ” Open Positions

Pharmacovigilance Roles

  • Pharmacovigilance Services Associate (1โ€“3 yrs)
  • Pharmacovigilance Services Sr Analyst (5โ€“8 yrs)
  • Pharmacovigilance Services Specialist (7โ€“11 yrs)
  • Delivery Operations Associate Manager (10โ€“14 yrs)

Clinical Data Management Roles

  • Clinical Data Services Associate (1โ€“3 yrs)
  • Clinical Data Services Sr Analyst (5โ€“8 yrs)
  • Clinical Data Services Specialist (7โ€“11 yrs)

Quality & Compliance Roles

  • Quality Assurance Associate Manager (10โ€“14 yrs)
  • Quality Assurance Manager (13โ€“18 yrs)

๐Ÿงช Key Responsibilities

Pharmacovigilance (PV)

  • ICSR case processing, data entry, and MedDRA coding
  • Signal detection and safety data review
  • Compliance with global regulatory requirements
  • Case follow-ups and submissions in safety databases

Clinical Data Management (CDM)

  • Clinical trial data collection, validation, and reconciliation
  • Site coordination and investigator communication
  • Database programming (SAS, RAVE, Oracle Clinical)
  • Data analysis and reporting

Quality Assurance (QA)

  • Conduct audits and ensure regulatory compliance
  • Manage CAPA and quality systems
  • Lead client audits and inspections
  • Implement quality governance frameworks

๐ŸŽ“ Qualifications

  • Bachelor of Pharmacy (B.Pharm) โ€“ mandatory for most roles
  • Master of Pharmacy (M.Pharm) โ€“ preferred for senior roles
  • MBBS / BDS / BTech / MSc โ€“ required for select roles
  • Strong understanding of:
    • Pharmacovigilance & Drug Safety
    • Clinical trials & regulatory guidelines
    • Tools like MedDRA, SAS, RAVE, Oracle Clinical

๐Ÿ’ผ Skills Required

  • Analytical thinking & problem-solving
  • Attention to detail (critical for PV/CDM roles)
  • Team collaboration and stakeholder management
  • Ability to work in rotational shifts
  • Regulatory compliance awareness

๐Ÿ’ฐ Salary (Estimated)

  • Associate (1โ€“3 yrs): โ‚น3.5 โ€“ โ‚น6 LPA
  • Sr Analyst (5โ€“8 yrs): โ‚น7 โ€“ โ‚น12 LPA
  • Specialist (7โ€“11 yrs): โ‚น12 โ€“ โ‚น18 LPA
  • Manager roles (10+ yrs): โ‚น18 โ€“ โ‚น30 LPA

(Actual salary depends on experience, skillset, and interview performance)


๐ŸŒŸ Why Join Accenture?

  • Global exposure in Life Sciences R&D
  • Structured career growth in Pharmacovigilance and Clinical Research
  • Opportunity to work with top biopharma clients
  • Strong learning ecosystem and certifications
  • Stable corporate environment with large-scale projects

๐Ÿ“ Job Locations

  • Bengaluru, Karnataka
  • Mumbai, Maharashtra

๐Ÿ“Œ How to Apply

Pharmacovigilance Roles

Clinical Data Management Roles

Quality & Compliance Roles

Share This Job

โœ… Job Details Copied!