Assoc Scientist, Lab Operations

IQVIA LLC

Indianapolis (IN)

On-site

USD 43,000 - 89,000

Full time

4 days ago
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Job summary

IQVIA Laboratories in Indianapolis, IN, is seeking a detail-oriented professional for routine laboratory testing and data analysis in drug development and clinical trials. You will document procedures and results in compliance with SOPs and regulatory requirements, supporting calibration, maintenance, and safety initiatives.

The role emphasizes preparing buffers, using LIMS for data uploads, and training staff while working with cross-functional teams to ensure data quality and project progress.

Qualifications

  • Associate degree in medical technology or equivalent required.
  • 6 months of experience in a regulated laboratory environment.
  • Proficient in preparing buffers and solutions.
  • Experience with automation or specialized lab instruments.
  • Proficient in routine calculations (averages, std dev, QC).
  • Certification as required by regulatory body.

Responsibilities

  • Perform and document analytical procedures per SOPs and regulations.
  • Analyze data, confirm results, and escalate anomalies.
  • Prepare buffers, solutions, and upload results to LIMS.
  • Calibrate and maintain laboratory equipment.
  • Support quality investigations and procedural updates.
  • Train lab personnel on routine procedures.
  • Communicate with cross-functional stakeholders on projects.
  • Support safety, quality, inventory, and 6S initiatives.

Skills

Laboratory techniques
Automation equipment
Data calculation
Regulatory compliance

Education

Associate's degree in medical technology

Tools

Laboratory equipment handling

Job description

Job Summary

Perform routine laboratory testing and analysis to generate reliable data for drug development and clinical trials research. Document procedures and results in accordance with standard operating procedures and applicable regulatory requirements.

What You’ll Be Doing
  • Perform and document analytical procedures in accordance with standard operating procedures and regulatory guidelines
  • Analyze routine data, confirm results are within acceptable tolerances, and escalte unusual findings or potential performance errors
  • Prepare buffers and solutions and support the upload of analytical results into the laboratory information management system
  • Perform and document assigned equipment calibration and maintenance activities
  • Assist with quality investigations, deviations, procedural updates, and the implementation of laboratory process changes
  • Train and guide laboratory personnel on routine procedures in areas of demonstrated competency
  • Communicate clearly and promptly with cross-functional stakeholders and represent the laboratory team on assigned projects
  • Support laboratory safety, quality, inventory, continuing education, and 6S initiatives
What We Are Looking For
  • An Associate's degree or educational equivalent in medical technology is required
  • 6 months of experience in a regulated laboratory environment
  • Proficiency with relevant laboratory techniques, including the preparation of buffers and solutions and the handling of batches and specimens
  • Experience using automation or specialized laboratory equipment
  • Proficiency with routine and some non-routine laboratory calculations, including averages, means, standard deviations, and quality control metrics
  • An applicable certification required by country, state, or other relevant regulatory body is required
  • Other equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role
  • Basic knowledge of the assigned technical area, laboratory systems, procedures, and applicable regulatory standards, such as Good Laboratory Practices
  • Knowledge of laboratory safety, infection-control practices, standard precautions, and hazardous chemical handling
  • Strong attention to detail and accuracy, with the ability to recognize unusual results and document work clearly
  • Ability to manage multiple tasks and collaborate effectively with laboratory colleagues and cross-functional stakeholders
  • Good computer skills, including proficiency with Microsoft Outlook, Word, and Excel
  • Ability to support the onboarding and hands-on training of laboratory personnel
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 $42,700.00 - $89,000.00. 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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