Senior Scientist, Large Molecule Bioanalytical

IQVIA • Indianapolis, IN

2d

About The Position

IQVIA Laboratories is seeking a Senior Scientist, Large Molecule Bioanalytical to provide technical leadership for complex large-molecule bioanalytical method development and serve as Primary Investigator on scientific client studies. The role involves conducting laboratory work, communicating study progress and results, and collaborating with clients and cross-functional teams to deliver scientifically rigorous solutions that support drug development programs.

The Senior Scientist designs and executes complex method-development experiments for large-molecule therapeutic candidates; evaluates and implements methods, technologies, and instrumentation; prepares technical reports, proposals, and protocols, including reports that may support FDA submissions; and analyzes and interprets experimental data, including statistical analysis. The role also manages multiple complex projects, mentors junior scientific staff, collaborates across functions to deliver client studies and deploy methods across programs, and maintains laboratory notebooks, equipment standards, and compliance with SOPs, regulatory requirements, and good documentation practices.

The position is with IQVIA Laboratories in Indiana. The stated annualized potential base pay range is $64,200 to $133,600; actual pay may vary based on qualifications, location, schedule, and other factors. Incentive plans, bonuses, or other compensation may be offered depending on the position. The company describes benefits and resources intended to support employees’ physical, mental, emotional, financial, and social well-being; further details are available through its benefits website.

Requirements

• Master's degree in a science field plus 8 or more years of experience, or an equivalent combination of education, training, and experience in a bioanalytical laboratory environment.
• Strong understanding of bioanalytical techniques used in drug development, including ADME concepts and experimental techniques applied to large molecules.
• Advanced proficiency with Microsoft Excel, including statistical data analysis, as well as PowerPoint, Word, instrument software, and scientific data-analysis programs.
• Ability to organize and execute multiple complex projects simultaneously with a high degree of independence and motivation.
• Effective scientific writing, presentation, interpersonal, and client communication skills.
• Ability to collaborate across departments, contribute to multidisciplinary discussions, and establish effective working relationships.
• Demonstrated everyday leadership, including the ability to mentor colleagues and contribute to safety and Six Sigma initiatives.
• Other equivalent combinations of education, training, and experience may be accepted in lieu of a degree.

Nice To Haves

• Ph.D. in Chemistry, Analytical Chemistry, Biochemistry, Chemical Biology, Biology, or a related field.
• Peer-reviewed scientific publications in a relevant field.
• Experience working with antibodies, antibody-drug conjugates, and oligonucleotide conjugates with payloads such as ASOs, PMOs, and siRNA.
• Experience with mass spectrometry, CE-SDS, SDS-PAGE, BCA, SEC-HPLC, and UV-visible spectroscopy.
• Experience evaluating the stability, potency, efficacy, and purity of therapeutic candidates used in in vitro and in vivo studies.

Responsibilities

• Serve as Primary Investigator on scientific client studies, conduct laboratory work, and communicate progress and results.
• Design and execute complex method-development experiments for large-molecule therapeutic candidates.
• Evaluate and implement new bioanalytical methods, technologies, and instrumentation for client programs.
• Prepare technical summary reports, proposals, and protocols, including reports that may support FDA submissions.
• Analyze and interpret data, including statistical analysis of experimental findings.
• Manage multiple complex technical projects and guide or mentor junior scientific staff.
• Collaborate across functions to deliver client studies and deploy methods across multiple programs.
• Maintain laboratory notebooks and equipment standards, and ensure compliance with applicable SOPs, regulatory requirements, and good documentation practices.

Benefits

• Benefits and resources supporting employees’ physical, mental, emotional, financial, and social well-being.
• Potential incentive plans, bonuses, and/or other forms of compensation, depending on the position offered.
• Health and welfare benefits may be offered.

What This Job Offers

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