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.
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.
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.
- 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.
- 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.