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Accenture Hiring Pharmacovigilance & Clinical Database Programming
🏢 Accenture
📍 Chennai & Bengaluru
💊 Pharmacovigilance
💻 Clinical Database Programming
🎓 1–8 Years
Accenture Careers has announced multiple openings in the Life Sciences R&D domain for professionals in Pharmacovigilance and Clinical Data Services.
These openings are ideal for candidates from Pharmacy, Life Sciences, Nursing, Physiotherapy, Ayurveda, and Engineering backgrounds looking to build careers in Drug Safety, ICSR Processing, Clinical Data Management, EDC Systems, MedDRA Coding, and Clinical Database Programming.
📋 Job Overview
- Company: Accenture
- Department: Life Sciences R&D
- Locations: Chennai & Bengaluru
- Employment Type: Full-Time
- Industry: Pharmacovigilance / Clinical Research / Clinical Data Management
- Experience: 1–8 Years
💰 Estimated Salary: ₹4 – ₹14 LPA
💊 Pharmacovigilance Services Associate – Chennai
- Experience: 1–3 Years
- Qualification: B.Pharm, BPT, BSc Nursing
- Department: Pharmacovigilance & Drug Safety Surveillance
📌 Key Responsibilities
- ICSR case identification and data entry
- MedDRA coding and case processing
- Safety database submissions and follow-ups
- Drug safety surveillance support
- Regulatory compliance and SOP adherence
- Cross-functional team collaboration
📚 Pharmacovigilance Learning Resources
👉 Entry Level Pharmacovigilance Quiz
👉 Drug Safety Analyst Quiz
👉 Top 100 Pharmacovigilance Interview Questions
👉 Pharmacovigilance Salary Guide
🧪 Pharmacovigilance Services Sr Analyst – Bengaluru
- Experience: 5–8 Years
- Qualification: Any Graduation, BAMS, MSc Life Sciences
- Department: Pharmacovigilance
📌 Key Responsibilities
- ICSR review and quality control
- Safety database validation
- Adverse event seriousness assessment
- Regulatory safety reporting
- Client communication and reconciliations
- Training and transition activities
💻 Clinical Data Services Associate – Bengaluru
- Experience: 1–3 Years
- Qualification: BE
- Department: Clinical Database Programming
📌 Key Responsibilities
- Develop and review edit checks
- Create patient profile listings and reports
- Support database validation activities
- Assist in EDC build and testing
- Ensure clinical trial data quality and compliance
- Work with SAS, Cognos, and J-Review tools
💻 Clinical SAS & CDM Resources
👉 Clinical SAS Programmer Quiz
👉 Base SAS vs PROC SQL
👉 Clinical SAS PDV Explained
👉 Clinical SAS vs Clinical Data Management
🌍 Why Join Accenture?
- Work with global pharmaceutical and biotech clients
- Exposure to pharmacovigilance and clinical trial operations
- Structured learning and career development
- Technology-driven healthcare projects
- Collaborative and inclusive work culture
- Strong growth opportunities in Life Sciences R&D
📄 Resume Tips
- Highlight pharmacovigilance or CDM experience clearly
- Mention MedDRA, EDC, SAS, or safety database exposure
- Add clinical research certifications if available
- Use ATS-friendly resume formatting
- Showcase communication and analytical skills
- Keep resume concise and professional
🎯 Preparation Resources
👉 CRA Quiz & Clinical Research Preparation
👉 Aptitude & Reasoning Quiz
👉 Data Analyst Interview Questions
🧩 Fun Learning & Career Growth
Improve your healthcare knowledge, analytical thinking, and interview preparation with our quizzes and healthcare puzzles.
🚀 Select Job Role & Apply
📌 Note Before You Apply:
Kindly read the complete job description carefully before applying. Make sure your qualifications, experience, and technical skills align with the selected role before proceeding.
Kindly read the complete job description carefully before applying. Make sure your qualifications, experience, and technical skills align with the selected role before proceeding.
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