Work from Home Clinical Tech Validation Role – Apply at Parexel


Remote Clinical Tech Validation Role – Apply at Parexel

📅 Published on: June 14, 2025


💼 Job Title: System Validation Services - Specialist II

🏢 Company: Parexel
👥 Experience: Minimum 3 Years
🌍 Location: Remote (Mohali, India)
🎓 Eligibility: B.Pharm / B.Tech / B.Sc in Life Sciences or IT, M.Pharm / M.Tech / M.Sc in Biotechnology, Pharmacy, or Computer Science / Pharm.D / Diploma in Clinical Research or IT Compliance
✅ Verified Job | Online Application Available


🏢 About Parexel

Parexel is a leading global clinical research organization (CRO) dedicated to improving global health. From clinical trials to regulatory consulting and market access, Parexel works with empathy and purpose to help bring life-changing therapies to market. Every team member plays a critical role in delivering better health outcomes.


📝 Job Description

The System Validation Services (SVS) Specialist II supports Parexel’s technology compliance by implementing standardized, risk-based validation strategies. The role ensures compliance with GxP guidelines while collaborating with internal teams across various technology lifecycles including:

  • Infrastructure Life Cycle
  • Software Development Life Cycle (SDLC)
  • Technology Quality Life Cycle

📌 Key Responsibilities

✅ Validation & Compliance

  • Lead validation efforts for Parexel systems using a risk-based approach
  • Guide teams to maintain GxP and regulatory compliance
  • Conduct Periodic Reviews of validated systems

✅ Risk Management

  • Support risk assessment for clinical technologies
  • Assist with audit readiness and inspection response

✅ Process Improvement

  • Contribute to Validation Framework Documents
  • Create training content for compliance processes

✅ Administrative Support

  • Maintain compliance documentation, timesheets, and records

🎓 Education & Experience

✔ Education:

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Computer Science, or related fields
  • Diploma holders in Clinical Research or IT Compliance are also eligible

✔ Experience:

  • 3+ years in clinical research, GCP, or computerized system validation (CSV)
  • Understanding of System Life Cycle (SLC) processes and GxP compliance
  • Familiarity with Lean Six Sigma, risk management, and project coordination

✔ Soft Skills:

  • Strong communication and problem-solving skills
  • Organized and proactive in a fast-paced, customer-driven environment
  • Ability to work independently and in cross-functional teams

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📥 How to Apply?

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