Associate BioServices Study Lead - Hybrid
IQVIA · Indianapolis, IN
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Role summary
This hybrid role involves scientific oversight of bioanalytical projects, including method development, validation, and sample analysis. The Associate Study Lead will serve as Principal Investigator for GLP studies, review regulatory documentation, manage project timelines, and coordinate with cross-functional teams. A bachelor's degree and three years of GLP laboratory experience are required, with proficiency in LC-MS, immunoassay, or related techniques.
What they're looking for
- Bachelor's degree in scientific field
- 3 years experience in GLP laboratory environment
- Knowledge of liquid chromatography-mass spectrometry or immunoassay techniques
- Experience with sample extraction and assay method development
- Strong written and verbal communication skills
- Ability to collaborate effectively across functional teams
- Excellent attention to detail and scientific judgment
What you'll be doing
- Provide scientific oversight for method development, validation, and sample analysis projects
- Serve as Principal Investigator for GLP studies and prepare regulatory documentation
- Review validation reports and bioanalytical data for regulatory compliance and quality
- Investigate failed runs, coordinate troubleshooting, and document findings
- Maintain customer communication, resolve discrepancies, and support project monitoring
Privacy & handoff
This role links to IQVIA'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.