We are seeking an Associate BioServices Study Lead - Hybrid to join IQVIA Laboratories at Indianapolis, IN.

Job Summary:

What You'll Be Doing:

• Provide scientific oversight for method development, method validation, and sample analysis projects
• Serve as Principal Investigator for GLP studies
• Prepare validation and sample analysis plans, approve experimental designs, and review data for regulatory compliance and scientific quality
• Review validation and bioanalytical reports for completeness and address findings from Quality Control and Quality Assurance reviews
• Monitor assigned projects, communicate status updates, and escalate schedule risks to management
• Investigate failed runs, coordinate method troubleshooting, assemble technical resources, and document investigation findings
• Maintain communication with customers, resolve sample discrepancies, coordinate customer visits, and support quote preparation
• Ensure projects are archived in accordance with IQVIA SOPs and comply with applicable Good Clinical Practice and Good Laboratory Practice standards
   

What We Are Looking For:

• Bachelor's Degree Scientific field required
• 3 years’ related experience. Equivalent combination of education, training and experience in GLP laboratory environment.
• Understanding of liquid chromatography combined with mass spectrometry, or in vitro and immunoassay techniques
• Experience with sample extraction, routine laboratory procedures, assay method development, and assay validation
   

The Knowledge, Skills and Abilities Needed for This Role:

• Ability to achieve results through effective collaboration with colleagues and cross-functional partners
• Excellent attention to detail, scientific judgment, and written and verbal communication skills
• Ability to interact effectively with internal and external clients while working to defined objectives and timelines
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
   

What We Offer You: