Study Support Specialist (GLP studies – Product Safety Labs)
EurofinsWhitefield, BangalorePosted a month agoA free account shows the apply link for every role and matches you to the ones that fit your resume.
About the role
Eurofins provides analytical testing and laboratory services across life sciences and other industries. This specialist supports Study Directors by coordinating GLP study documentation, data quality reviews, timelines, samples, and regulatory-ready study records.
What you'll do
- Gather study requirements and details with laboratory staff
- Review laboratory data and study records for accuracy and completeness
- Monitor study milestones, deliverables, risks, and deadlines
- Coordinate GLP protocols, amendments, and study documentation
- Maintain audit-ready study files and tracking systems
- Prepare study data packages and technical writing materials
Skills
Must have
- Good laboratory practice
- Preclinical studies
- Clinical trials
- Regulatory requirements
- Technical writing
- Quality control
- Study documentation
Who it's for
- Education
- Master's degree
- Degree
- pharmacology, toxicology, science
- Experience
- 5 to 7 years
- Domain
- life sciences testing
About Eurofins
Eurofins has 97 open roles in Bangalore, at Eurofins IT Solutions India (Global Delivery Centre). See every Eurofins role.
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