Looking for a Veeva Vault job in India or a remote clinical research job? A leading global CRO, Syneos Health, is hiring a Regulated Systems Document Analyst for a remote India position.

This opportunity is ideal for B.Pharm, M.Pharm, Life Sciences, and Clinical Research graduates seeking careers in clinical data management, regulatory systems, and Veeva Vault operations. If you have strong attention to detail and want to work in a regulated pharma environment, this role offers excellent exposure.

🔍 Job Overview

• Role: Regulated Systems Document Analyst
• Location: Remote (India)
• Job ID: 15496
• Industry: Clinical Research / Pharma / CRO
• Employment Type: Full-time

📌 Key Responsibilities

• Manage end-to-end study tracking within Veeva Vault systems
• Perform data entry and updates ensuring accurate project records
• Generate, format, and maintain system reports
• Conduct quality checks (QC) between source systems and Vault
• Support clinical project timelines and milestones
• Coordinate with cross-functional teams for issue resolution
• Maintain high compliance standards in regulated environments
• Improve tracking processes and documentation systems

🎓 Qualifications Required

• Bachelor’s degree in:
  • Pharmacy (B.Pharm / M.Pharm)
  • Life Sciences / Biology / Chemistry
  • Clinical Research
• Skills & Experience:
  • Knowledge of Veeva Vault (Clinical/RIM modules)
  • Experience with CTMS or document management systems
  • Strong Excel and reporting skills
  • Excellent attention to detail and data accuracy
  • Fluent in English communication
  • Ability to manage multiple tasks and deadlines

💼 Preferred Skills

• Experience in regulated pharma or clinical environments
• Familiarity with clinical trial systems
• Strong organizational and time management skills
• Ability to work independently in remote settings

💰 Salary (Estimated)

• ₹4.5 LPA – ₹7.5 LPA (based on experience and skills)

🌟 Why Join Syneos Health?

• Work with a global clinical research organization (CRO)
• Exposure to Veeva Vault and regulated systems
• Opportunity to build a career in clinical operations & regulatory domains
• Remote work flexibility across India
• Collaborate on global pharma projects

📥 How to Apply

Application Link