Associate Validator II at Jobgether

, , India -

Full Time

Start Date

Immediate

Expiry Date

02 Oct, 26

Salary

0.0

Posted On

04 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

EDC Systems, Validation Documentation, Test Execution, GCP Compliance, ICH Guidelines, SOP Adherence, Data Integrity, Metrics Tracking, Clinical Study Operations, Quality Assurance, Cross-functional Collaboration, Technical Writing

Industry

Internet Marketplace Platforms

Description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Validator II based in India. This is a detail-oriented, quality-focused role supporting global clinical and validation operations within a regulated environment. You will be responsible for ensuring accuracy, consistency, and compliance across validation documentation and controlled study materials used in global EDC (Electronic Data Capture) systems. The role involves working closely with project teams to support validation activities, documentation handling, and test execution in line with strict industry standards. You will play a key part in maintaining data integrity by ensuring all processes align with SOPs, GCP, and ICH guidelines. The environment is structured, highly regulated, and deadline-driven, requiring strong attention to detail and a methodical working style. You will also contribute to continuous improvement efforts by supporting metrics tracking and validation reporting. This position is ideal for someone who thrives in precise, process-driven work and enjoys contributing to high-impact healthcare and clinical research initiatives. \n Accountabilities: Support project teams in validation and documentation activities related to global EDC systems and clinical study operations. Receive, log, scan, and manage contractual, validation, and controlled study documentation with accuracy and consistency. Assist in the creation, production, printing, tracking, and maintenance of study-related documents. Execute validation test scripts and accurately document results in line with defined procedures. Ensure all work complies with SOPs, GCP, and ICH regulatory guidelines while maintaining high quality standards. Maintain validation metrics and support reporting activities to ensure process transparency and performance tracking. Assist in special projects and additional operational tasks as assigned by management. Requirements: Bachelor’s degree in life sciences, health sciences, information technology, or related field, or equivalent relevant experience. Minimum 3 years of experience in validation within a global CRO, pharmaceutical, or regulated healthcare environment. Strong attention to detail with a methodical and structured approach to work. Ability to work under pressure while meeting strict deadlines in a quality-driven environment. Strong communication skills and ability to collaborate effectively within cross-functional project teams. Comfortable working with multiple systems and adapting to evolving tools and technologies. Fluent written and verbal English communication skills. High level of self-motivation, reliability, and consistency in executing defined processes. Benefits: Fully remote working arrangement based in India. Opportunity to work in a global, regulated clinical research environment. Exposure to international projects in healthcare, pharma, and life sciences validation. Structured work environment with clear processes, SOPs, and quality frameworks. Opportunity to develop expertise in validation, compliance, and clinical documentation systems. Collaborative team culture focused on quality, precision, and continuous improvement. Stable full-time role within a mission-driven organization supporting healthcare innovation. \n How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1

Responsibilities

Support global clinical operations by managing validation documentation and executing test scripts for Electronic Data Capture (EDC) systems. Ensure all processes maintain data integrity and comply with SOP, GCP, and ICH regulatory guidelines.