Associate Principal Scientist, Large Molecule Bioanalytical

Q² Solutions; Indianapolis (IN); On-site; USD 80,200 - 167,200; Full time

Benefits offered by this job

Comprehensive benefits programs

Employee well-being resources

Job summary

Q² Solutions in Indianapolis is seeking an Associate Principal Scientist, Large Molecule Bioanalytical. In this role, you will lead complex method development, working closely with clients to advance drug development programs.

The ideal candidate will possess a Ph.D. or equivalent experience in Chemistry or a related field, with a strong focus on bioanalytical techniques, especially LCMS. The position promises a comprehensive benefits package and a supportive work environment.

Qualifications

• Ph.D. or Master’s degree in a relevant field with extensive experience in a bioanalytical laboratory.
• Strong understanding of bioanalytical techniques applied to drug development.
• Experience in developing proteomics workflows.

Responsibilities

• Serve as a Primary Investigator on scientific client studies.
• Design and execute complex method development experiments.
• Manage multiple complex technical projects and guide junior staff.

Skills

Bioanalytical techniques

Liquid Chromatography-Mass Spectrometry (LCMS)

Advanced computer skills

Organizational skills

Communication skills

Education

Ph.D. in Chemistry, Biochemistry, or related field

Master’s degree plus 7 years of experience

Tools

Microsoft Excel

PowerPoint

Word

Job description

We are seeking an Associate Principal Scientist, Large Molecule Bioanalytical to join IQVIA Laboratories in 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.

As an individual contributor with advanced comprehensive knowledge of Bioanalysis, you will provide technical leadership on complex method development (LCMS/HRMS) and collaborate directly with clients on solutions for drug development programs.

What You’ll Be Doing

• Serving as a Primary Investigator on scientific client studies, carrying out laboratory work and communicating progress and results.
• Designing and executing complex method development experiments utilizing Separation Sciences, Liquid Extraction, and Hybrid Assays.
• Recommending and evaluating new technologies, specifically focusing on Sciex and HRMS platforms.
• Writing technical summary reports for clients, which may be used for FDA submissions, and reviewing reports drafted by junior staff.
• Drafting study proposals and protocols for client review and approval.
• Recommending and evaluating new technologies and instrumentation.
• Managing multiple complex technical projects and guiding junior staff.
• Working proactively across functions to ensure effective project delivery and method deployment.

What We Are Looking For

• Ph.D. in Chemistry, Analytical Chemistry, Biochemistry, Chemical Biology, Biology, or related field (preferred).
• Master’s degree in a science field plus 7 years of experience in a bioanalytical laboratory environment.
• Strong understanding of bioanalytical techniques applied to the drug development industry, specifically LCMS (Liquid Chromatography-Mass Spectrometry). HRMS experience is highly preferred.
• Knowledge and experience in developing proteomics workflows, including LFQ, TMT, AQUA, middle-down, and bottom-up techniques.
• Other equivalent combination of education, training, and experience may be accepted in lieu of degree.

The Knowledge, Skills, And Abilities Needed For This Role

• Advanced computer skills, including proficiency with Microsoft Excel, PowerPoint, Word, and other programs supporting experimental instruments and data analysis.
• Effective organizational, interpersonal, and time management skills.
• Strong communication and presentation skills.
• Ability to manage and execute multiple tasks or projects simultaneously.

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, 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 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

The potential base pay range for this role, when annualized, is $80,200.00 - $167,200.00. 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.