📢 Multiple Life Sciences Openings at Accenture
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✔ Verified by Medical Jobs India
Accenture Life Sciences Hiring – Multiple Roles
🏢 Accenture
📍 Bengaluru, Chennai, Mumbai & Gurugram
💊 PV & CDM
💼 0–11 Years
Accenture is hiring across its Life Sciences division for multiple openings in Pharmacovigilance, Drug Safety, Clinical Data Management, SAS Clinical Programming, and Project Management. These opportunities are ideal for Pharmacy, Clinical Research, Medical, and Life Sciences professionals seeking careers with a global healthcare consulting leader.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company | Accenture |
| Total Openings | 9 Roles |
| Locations | Bengaluru, Chennai, Mumbai, Gurugram |
| Experience | 0–11 Years |
| Industry | Life Sciences & Clinical Research |
| Employment Type | Full-Time |
💊 Pharmacovigilance Services Associate
- Location: Bengaluru
- Experience: 0–3 Years
- Qualification: B.Pharm, M.Pharm
- ICSR Processing
- Case Intake & Data Entry
- MedDRA Coding
- Drug Safety Operations
- Regulatory Compliance
🩺 Pharmacovigilance Services Specialist
- Location: Chennai
- Experience: 7–11 Years
- Qualification: MBBS, MD
- Medical Review
- Signal Detection
- Risk Assessment
- Global Safety Regulations
- Safety Oversight Activities
📊 Clinical Data Services Analyst
- Location: Bengaluru
- Experience: 3–5 Years
- Qualification: MSc
- Clinical Data Management
- Medidata RAVE EDC
- Data Validation & Cleaning
- Clinical Database Management
📈 Clinical Data Services Associate
- Location: Mumbai
- Experience: 1–3 Years
- Qualification: B.Pharm, MSc, BE
- Base SAS
- Clinical Data Review
- Clinical Research Support
- Data Quality Management
🚀 Program / Project Management Lead
- Location: Gurugram
- Experience: 7.5+ Years
- Qualification: Graduate (15 Years Education)
- Stakeholder Management
- Project Governance
- Risk Management
- Team Leadership
⭐ Key Skills
- Pharmacovigilance
- Drug Safety
- ICSR Processing
- MedDRA Coding
- Clinical Data Management
- Medidata RAVE
- Base SAS
- Regulatory Compliance
- Project Management
- Clinical Research
🌟 Why Join Accenture?
- Global Life Sciences project exposure.
- Career opportunities across PV, CDM, and Regulatory functions.
- Training and certification programs.
- International client exposure.
- Strong growth opportunities.
- Competitive compensation and benefits.
📈 Career Path
- Pharmacovigilance Associate
- Clinical Data Associate
- Drug Safety Specialist
- Clinical Data Analyst
- Senior PV Specialist
- Project Manager
- Program Management Lead
📝 Resume Tips
- Highlight Pharmacovigilance, Clinical Data Management, SAS, or Project Management experience.
- Mention Argus, MedDRA, Medidata RAVE, or EDC systems if applicable.
- Showcase ICSR processing, data cleaning, reconciliation, and regulatory compliance activities.
- Include certifications related to PV, CDM, SAS, or Clinical Research.
- Quantify achievements wherever possible.
- Keep your resume ATS-friendly and role-specific.
🎯 Interview Preparation Tips
- Review Pharmacovigilance and ICSR workflows.
- Understand MedDRA coding and safety reporting timelines.
- Revise Clinical Data Management and EDC concepts.
- Practice SAS and clinical data-related questions.
- Understand GCP, ICH, and regulatory requirements.
- Prepare project management examples if applying for leadership roles.
- Research Accenture Life Sciences services.
❓ Common Interview Questions
- What is Pharmacovigilance?
- What is an ICSR?
- What is MedDRA coding?
- What is Medidata RAVE?
- What is data reconciliation in CDM?
- Explain SAE reporting timelines.
- What is Base SAS used for in Clinical Research?
- How do you manage data quality?
- Why do you want to join Accenture?
- Describe a challenging project you handled.
❓ Frequently Asked Questions (FAQ)
Q1. How many openings are available?
Accenture is hiring for 9 different Life Sciences roles.
Q2. What experience range is required?
Roles are available for candidates with 0–11 years of experience.
Q3. Which locations are hiring?
Bengaluru, Chennai, Mumbai, and Gurugram.
Q4. Are Pharmacy candidates eligible?
Yes, B.Pharm, M.Pharm, Pharm.D, MSc, MBBS, and MD candidates are eligible depending on the role.
Q5. Which domains are covered?
Pharmacovigilance, Drug Safety, Clinical Data Management, SAS Programming, and Project Management.
📝 How to Apply
- Select the role that best matches your experience and qualification.
- Update your resume with relevant PV, CDM, SAS, or project experience.
- Highlight certifications and technical skills.
- Review the job description carefully before applying.
- Submit your application through the appropriate link below.
👉 Step-by-Step Guide: How to Apply for Healthcare & Pharma Jobs
🚀 Apply Now
Apply – PV Associate 1 Apply – PV Associate 2 Apply – PV Associate 3 Apply – PV Associate 4 Apply – PV Associate 5 Apply – PV Specialist Apply – Project Management Lead Apply – Clinical Data Analyst Apply – Clinical Data Associate
📚 Related Resources from HiTechPlus
👉 Pharmacovigilance Resources
👉 Clinical Research Resources
👉 SAS Programming Resources
👉 Clinical Data Management Resources
👉 CRA Quiz
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