Accenture Hiring Clinical Data (SAS), Regulatory & Pharmacovigilance Professionals
Accenture is hiring for multiple Life Sciences and Healthcare roles across Clinical Data Services, Regulatory Operations, and Pharmacovigilance departments in India.
These opportunities are ideal for candidates interested in Clinical Data Management, SAS Clinical, Regulatory Affairs, Pharmacovigilance, Safety Writing, Drug Safety Operations, and Global Healthcare Projects.
📋 Accenture Life Sciences Hiring Overview
- Company: Accenture
- Locations: Mumbai & Bengaluru
- Industry: Life Sciences / Healthcare / Clinical Research
- Job Type: Full-Time
- Qualification: B.Pharm / M.Pharm / BE / MSc
- Experience: 1–5 Years
🏢 About Accenture
Accenture is a global professional services company specializing in digital, cloud, AI, consulting, technology, and operations across more than 120 countries.
The company’s Life Sciences R&D division supports pharmaceutical and biotechnology organizations in Clinical Trials, Pharmacovigilance, Regulatory Affairs, Clinical Data Management, and Drug Safety Operations.
📊 Clinical Data Svs Associate – Mumbai
🎓 Qualification
- BE / MSc / B.Pharm
🧑💻 Experience Required
- 1–3 Years
📌 Key Responsibilities
- Manage and process clinical trial datasets
- Support clinical data validation and analysis
- Handle data integration and standardization activities
- Ensure regulatory compliance and data quality
- Collaborate with internal clinical teams
- Perform reporting and operational tasks
⭐ Required Skills
- Clinical Data Management knowledge
- SAS Clinical understanding
- Analytical and problem-solving abilities
- Team collaboration skills
- Ability to work in rotational shifts
📂 LifeScience Regulatory Svs Analyst – Bengaluru
🎓 Qualification
- B.Pharm / M.Pharm
🧑💻 Experience Required
- 3–5 Years
📌 Key Responsibilities
- Support global regulatory submissions and filings
- Handle CMC submissions and annual reports
- Process electronic regulatory submissions
- Coordinate regulatory documentation activities
- Ensure compliance with global regulatory standards
- Manage lifecycle submission activities
⭐ Required Skills
- Regulatory Affairs experience
- Stakeholder management
- Client communication abilities
- Strong documentation handling
- Adaptability and deadline management
💊 Pharmacovigilance Services Analyst – Bengaluru
🎓 Qualification
- M.Pharm
🧑💻 Experience Required
- 3–5 Years
📌 Key Responsibilities
- Prepare adverse event case narratives
- Develop safety reports for clinical studies
- Author and review Risk Management Plans (RMPs)
- Perform peer quality reviews
- Support pharmacovigilance documentation activities
- Ensure compliance with SOPs and PV regulations
⭐ Required Skills
- Pharmacovigilance operations expertise
- Safety writing experience
- Risk Management Plan preparation
- Clinical safety documentation knowledge
- Strong attention to detail
🌍 Benefits of Working at Accenture
- Global work environment
- Career growth opportunities
- Learning and development programs
- Exposure to global pharmaceutical clients
- Technology-driven healthcare projects
- Inclusive workplace culture
- Cross-functional industry experience
📄 Resume & Interview Tips
- Highlight SAS, Regulatory, or Pharmacovigilance experience
- Mention compliance, reporting, and documentation skills
- Showcase stakeholder communication abilities
- Keep resume ATS-friendly and concise
- Add project and operational experience clearly
🚀 Select Role & Apply
Kindly read the complete job description carefully before applying. Make sure your Clinical Data, Regulatory Affairs, or Pharmacovigilance experience aligns with the selected role before proceeding.
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