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Accenture Hiring for 9 Pharmacovigilance & Clinical Data Roles | 0 – 11 Years

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Accenture Careers has announced multiple hiring opportunities for professionals in Pharmacovigilance, Drug Safety, Clinical Data Management, SAS Clinical Programming, and Project Management across India. These openings are ideal for B.Pharm, M.Pharm, MSc, BE, MBBS, and MD candidates seeking careers in the pharmaceutical, clinical research, and life sciences sectors.

The company is recruiting for 9 positions across Bengaluru, Chennai, Mumbai, and Gurugram within its Life Sciences R&D division, supporting global pharmaceutical and biotechnology clients.

Key Highlights

  • Company: Accenture
  • Industry: Life Sciences, Clinical Research, Pharmacovigilance
  • Total Openings: 9 Roles
  • Locations: Bengaluru, Chennai, Mumbai, Gurugram
  • Experience Required: 1โ€“11 Years
  • Employment Type: Full-Time
  • Department: Clinical, Pharmacovigilance & Regulatory Services

Available Positions

1. Pharmacovigilance Services Associate

Location: Bengaluru
Experience: 0 โ€“3 Years
Qualification: B.Pharm, M.Pharm

2. Pharmacovigilance Services Specialist

Location: Chennai
Experience: 7โ€“11 Years
Qualification: MBBS, MD

3. Program/Project Management Lead

Location: Gurugram
Experience: 7.5+ Years
Qualification: Any Graduate (15 Years Full-Time Education)

4. Clinical Data Services Analyst

Location: Bengaluru
Experience: 3โ€“5 Years
Qualification: MSc

5. Clinical Data Services Associate

Location: Mumbai
Experience: 1โ€“3 Years
Qualification: B.Pharm, MSc, BE


Job Responsibilities

Depending on the role, selected candidates will be responsible for:

Pharmacovigilance & Drug Safety

  • Case intake and case processing of ICSRs
  • Adverse event data entry and reconciliation
  • MedDRA coding and medical review support
  • Safety database management
  • Regulatory reporting and submissions
  • Follow-up activities and case lifecycle management
  • Signal detection and risk assessment support
  • Compliance with global pharmacovigilance regulations

Clinical Data Management

  • Clinical trial data review and validation
  • Data cleaning and discrepancy management
  • Medidata RAVE EDC operations
  • Clinical database maintenance
  • Data quality review and reporting
  • Support clinical study conduct and analysis

SAS Clinical Data Services

  • Clinical data integration and analysis
  • Base SAS programming support
  • Clinical domain data processing
  • Regulatory-compliant data management

Project Management

  • Lead pharmacovigilance programs and teams
  • Stakeholder communication and governance
  • Risk management and mitigation
  • Delivery oversight and project execution
  • Strategic planning and operational excellence

Required Qualifications

Pharmacovigilance Services Associate

  • Bachelor of Pharmacy (B.Pharm)
  • Master of Pharmacy (M.Pharm)
  • 1โ€“3 years experience in Drug Safety or Pharmacovigilance

Pharmacovigilance Services Specialist

  • MBBS or MD
  • Medical review experience in Pharmacovigilance
  • Strong understanding of global safety regulations

Clinical Data Services Analyst

  • MSc
  • Experience with Medidata RAVE EDC
  • Knowledge of Clinical Data Management processes

Clinical Data Services Associate

  • B.Pharm, MSc, or BE
  • Base SAS knowledge preferred
  • Clinical research domain understanding

Program/Project Management Lead

  • Minimum 7.5 years of Pharmacovigilance experience
  • Team leadership experience
  • Strong stakeholder management skills

Preferred Skills

  • Pharmacovigilance & Drug Safety Surveillance
  • ICSR Processing
  • MedDRA Coding
  • Argus Safety Database
  • Clinical Data Management
  • Medidata RAVE EDC
  • Base SAS Programming
  • Regulatory Compliance
  • Risk Management
  • Team Collaboration
  • Communication Skills
  • Problem Solving

Why Join Accenture?

Accenture is one of the world’s leading professional services organizations with nearly 800,000 employees serving clients across 120+ countries.

Employee Benefits

  • Global Life Sciences exposure
  • Career growth opportunities
  • Training and upskilling programs
  • International project experience
  • Diverse and inclusive workplace
  • Exposure to advanced digital technologies
  • Competitive compensation and benefits
  • Opportunities in Pharmacovigilance, Clinical Research, and Data Sciences

How to Apply

Application Link For Pharmacovigilance Services Associate

Application Link For Pharmacovigilance Services Associate

Application Link For Pharmacovigilance Services Associate

Application Link For Pharmacovigilance Services Associate

Application Link For Pharmacovigilance Services Associate

Application Link For Pharmacovigilance Services Specialist

Application Link For Program/Project Management Lead

Application Link For Clinical Data Services Analyst

Application Link For Clinical Data Services Associate

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