Associate Validator II Clinical Administration at Fortrea Apply Now!
Job Details
- Company: Fortrea
- Position: Associate Validator II (Clinical Administration)
- Location: Bangalore
- Experience Required: 2-3 years
- Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
- Application Mode: Online
Key Responsibilities
✅ Study Documentation & Tracking – Maintain, organize, and track study materials and controlled documents.
✅ Validation Support – Assist project teams with validation tasks and ensure regulatory compliance.
✅ Test Script Execution – Develop, execute, and document validation test scripts with accuracy.
✅ Regulatory Compliance – Ensure adherence to GCP (Good Clinical Practice) & ICH (International Council for Harmonisation) guidelines.
✅ Quality Control – Maintain validation metrics and support quality management activities.
✅ Project Coordination – Efficiently prioritize workload to meet project timelines.
Associate Validator II Clinical Administration at Fortrea
Eligibility Criteria
Education:
- Bachelor’s or Master’s degree in Pharma, Science, Life Sciences, or a related field.
Experience:
- 2-3 years of experience in validation, quality control, or regulatory compliance in the pharmaceutical or clinical research industry. Associate Validator II Clinical Administration at Fortrea
Key Skills Required:
✅ Familiarity with Electronic Data Capture (EDC) systems.
✅ Knowledge of regulatory documentation & compliance regulations.
✅ Understanding of GCP/ICH guidelines.
✅ Strong organizational skills with attention to detail.
✅ Excellent verbal & written communication skills.
Why Join Fortrea?
🌍 Work with a global CRO that operates in 100+ countries.
📈 Career advancement opportunities in clinical research & validation.
💼 Competitive salary & benefits (including insurance).
🚀 Work on challenging projects in drug & device development.
⚖ Great work-life balance & time management support.
How to Apply?
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