Research Associate

IQVIA LLC; Durham (NC); On-site; USD 54,000 - 112,000; Full time

Job summary

IQVIA Laboratories in Durham, NC is seeking a Research Associate to perform technical laboratory procedures supporting sample analysis, method development, and validation. You will generate high-quality data, document results, troubleshoot issues, and contribute to continuous improvement in line with procedures and regulatory guidelines.

The role requires a Bachelor's in biology, chemistry, or related field, with 0-2 years of related experience or a Master's degree.

Qualifications

• Bachelor's degree in biology, chemistry or related field is required.
• Basic knowledge of method development and analytical techniques.
• Understanding of sample handling and preparation.
• Working knowledge of regulatory agency standards.

Responsibilities

• Perform and document analytical procedures in accordance with company procedures and regulatory requirements.
• Execute routine methods and assays under moderate supervision, supporting method development and validation activities.
• Contribute to technical discussions, experimental design, data review, and sponsor inquiries.
• Troubleshoot laboratory processes and equipment to improve data quality and turnaround times.
• Prepare data analysis results for upload to LIMS under senior staff guidance.
• Prepare buffers and solutions for analysis.
• Calibrate, maintain, and train on lab equipment; ensure safety and quality initiatives.

Skills

Data analysis

Equipment troubleshooting

Analytical techniques

Communication skills

Education

Bachelor's Degree in Biology, Chemistry, or related field

Tools

Microsoft Excel

Microsoft PowerPoint

Microsoft Word

Job description

Job Summary

The Research Associate performs technical laboratory procedures and experimental activities in support of sample analysis, method development, and validation. This role contributes to high-quality data generation, documentation, troubleshooting, and continuous improvement in accordance with company procedures and regulatory guidelines.

What You'll Be Doing

• Perform and document analytical procedures in accordance with company procedures, regulatory requirements, and corporate guidelines
• Execute routine methods and assays under moderate supervision, supporting method development and validation activities
• Contribute to technical discussions, experimental design, data review, and responses to sponsor inquiries
• Troubleshoot laboratory processes and equipment issues to improve data quality, reduce costs, and support turnaround times
• Prepare data analysis results for upload to LIMS under the guidance of senior staff
• Prepare buffers and solutions for analysis, as required
• Perform and document calibration, maintenance, and hands‑on training activities for laboratory equipment and personnel
• Support laboratory safety, 6S requirements, continuing education, and quality initiatives

What We Are Looking For

• Bachelor's Degree in Biology, Chemistry, or a related field is required
• Bachelor's degree plus 1-2 years of related experience in method development or specific methodology area or a Masters degree; or equivalent combination of education, training and experience.; Degree in chemistry, biology, or related field
• Basic knowledge of method development and analytical techniques for the assigned technical area, including principles, theories, concepts, and instrumentation
• Understanding of sample handling and preparation
• Working knowledge of regulatory agency standards within the area of responsibility
• Knowledge of laboratory safety and infection control procedures and practices, including standard precautions and hazardous chemical handling
• Other equivalent combination of education, training, and experience may be accepted in lieu of degree

The Knowledge, Skills and Abilities Needed for This Role

Strong technical knowledge of complex analytical techniques and the science supporting the analysis

Proficiency with data analysis techniques and calculations

Ability to troubleshoot laboratory equipment and resolve process issues

Good computer skills, including proficiency with Microsoft Excel, PowerPoint, and Word

Effective organizational, interpersonal, communication, and presentation skills

Ability to handle multiple tasks simultaneously while maintaining strong attention to detail and accuracy

Ability to establish and maintain effective working relationships with coworkers, managers, and clients

Ability to maintain a degree of independence to complete assigned tasks and projects

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 IQVIA 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.

The potential base pay range for this role, when annualized, is $53,700.00 - $111,800.00. 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 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.

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.

Thank you for your interest in growing your career with us.