Scientist - ADME

IQVIA • Indianapolis, IN

1d • Onsite

About The Position

We are seeking Scientist - ADME to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Perform hands-on laboratory assays using automated liquid handling workflows to support sample analysis, method development, and validation. Generate high-quality data and documentation that meet turnaround time expectations and regulatory and corporate requirements.

Requirements

• Bachelor’s degree in Biology, Chemistry, or a related field with 1–2 years of relevant laboratory experience, or a Master’s degree (or equivalent combination of education, training, and experience)
• Experience performing in vitro assays and plate-based screening workflows, including sample handling and preparation
• Experience with automated liquid handling (ALH), preferably Tecan platforms, plus proficiency with Microsoft Excel, Word, and PowerPoint
• Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
• Working knowledge of method development concepts, analytical techniques, and the role of assays within the drug development process
• Strong attention to detail with the ability to produce accurate, compliant documentation and meet timeline-driven deliverables
• Ability to troubleshoot equipment and processes, communicate clearly, and collaborate effectively within a cross-functional laboratory team

Responsibilities

• Execute and document analytical and in vitro screening procedures in accordance with company procedures and applicable regulatory guidelines
• Operate Tecan-based automated liquid handling workflows to run routine assays and support day-to-day lab throughput
• Prepare samples, buffers, and solutions; perform accurate pipetting, reagent handling, and plate-based assay setup
• Support method development, assay optimization, and validation activities under moderate supervision
• Perform routine data review and basic statistical/data calculations to confirm results meet acceptance criteria
• Troubleshoot assay performance and laboratory equipment issues; escalate abnormal results or potential quality concerns promptly
• Enter, format, and prepare results for upload to LIMS and ensure documentation is complete, traceable, and audit-ready
• Perform calibration and maintenance of laboratory equipment and provide hands-on training to colleagues in areas of proven competency

Benefits

• We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level