Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Associate Validator II – Fortrea

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Self-Help & Motivational

careers

Data Management

Location

Bangalore, India / Remote (India)

Job Type

Full-time (Remote)

Experience Required

3+ years of validation experience in a Global CRO, Pharmaceutical, or Clinical Research organization.
Experience with Electronic Data Capture (EDC) validation and clinical systems is preferred.

Estimated Salary Package (Market Standard)

₹8 – ₹14 LPA (approx.), depending on experience, technical expertise, and interview performance.

Job Overview

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Management

Pharmaceutical

Career

management

Pharmacy

Corporate Training

Pharmaceuticals & Biotech

The Associate Validator II supports Global EDC Solutions by managing validation documentation, executing validation activities, and ensuring compliance with Quality Management,



Valuable Clinical Practice (GCP), and ICH guidelines. The role involves creating and executing validation test scripts, maintaining controlled documentation, and supporting project teams in validation-related tasks.

Key Responsibilities

Validation & Testing

Create, execute, and document validation test scripts.
Support validation activities for Electronic Data Capture (EDC) systems.
Record and maintain validation test results accurately.
Ensure validation deliverables meet quality standards.

Documentation Management

Manage validation and contractual documentation.
Create, print, track, and maintain study documentation and controlled documents.
Maintain accurate records of all validation activities.
Ensure documentation complies with project requirements and SOPs.

Project Support

Support project teams with validation-related activities.
Prioritize assigned tasks to meet project timelines.
Assist in maintaining val

📌 Associate Validator II (Bengaluru)
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📍 Bengaluru