Associate Validator II Clinical Administration at Fortrea Apply Now!

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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.