Study Support Specialist (GLP studies – Product Safety Labs)
Eurofins · Bengaluru, India
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Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
This role links to Eurofins's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.