Associate Validator II

This is a fully remote position, open to applicants in India.

📋 Description

• Act as a key member of the project team, primarily responsible for the documentation requirements related to Global EDC Solutions tasks.

• Accept, log, and digitize contractual and validation documents.

• Support project teams with validation activities.

• Generate, produce, print, and monitor study documentation and controlled documents.

• Develop and implement validation test scripts while documenting the test outcomes.

• Ensure high-quality standards in all work produced.

• Organize workload effectively to meet designated deadlines.

• Assist in the upkeep of validation metrics.

• Conduct activities in accordance with Fortrea SOPs, project-specific guidelines, Quality Management, and GCP/ICH standards.

• Keep precise records of all work carried out.

• Undertake additional duties and special projects as assigned.

⛳️ Requirements

• A university or college degree in life sciences, health sciences, information technology, or a related field from a recognized accredited institution, or certification in allied health professions.

• Proficient in English, both written and spoken.

• 2–4 years of experience in Clinical Data Management (CDM) and Electronic Data Capture (EDC) testing.

• Practical knowledge of Rave and Veeva platforms.

• A systematic, organized, and meticulous approach to tasks with a strong attention to detail.

• Excellent focus and concentration abilities.

• Capability to perform under pressure and adhere to tight deadlines.

• Strong communication skills and the ability to collaborate effectively within a team.

• Relevant and equivalent experience may be accepted in place of formal educational qualifications.

• Willingness to work flexible shift-based hours.

🏝️ Benefits

• Opportunity for remote work.

• Flexible shift-based working hours.

• Equal Employment Opportunity (EEO) and accommodations support.