Job Description

We are seeking a Scientist/Associate 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.

What You'll Be Doing:

• 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

What We Are Looking For:

• 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

The Knowledge, Skills and Abilities Needed for This Role:

• 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

What We Offer You:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. 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.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $51,800.00 - $108,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.