Study Support Specialist (GLP studies - Product Safety Labs) in Bangalore, भारत

Eurofins seeks a Study Support Specialist to assist Study Directors in Good Laboratory Practice (GLP) non-clinical safety studies. The role involves coordinating study documentation, conducting quality control reviews, managing logistics, and ensuring regulatory compliance throughout the study lifecycle.

Responsibilities

• Gather study requirements and design details from laboratory staff for study initiation
• Conduct quality control reviews of laboratory data, worksheets, and records for completeness
• Monitor study milestones and critical path activities to identify risks and delays
• Coordinate development, review, and issuance of protocols and study documentation
• Maintain audit-ready study files and support data package compilation for reporting

Requirements

• Master's degree in pharmacology, toxicology, or related science field
• 5-7 years of pre-clinical studies, IND-enabling studies, or IND filing experience
• Knowledge of GLP regulatory requirements and standards
• Strong organizational and detail-oriented skills with accuracy
• Excellent written, verbal, and presentation communication abilities
• Proficiency in data management and technical writing
• Ability to manage multiple tasks and handle workplace stress