Senior Scientist, Large Molecule Bioanalytical
IQVIA
Summary
Provide technical leadership for complex large-molecule bioanalytical method development and serve as Primary Investigator on scientific client studies. Collaborate with clients and cross-functional teams to deliver scientifically rigorous solutions supporting drug development programs.
Job description
Job Summary
Provide technical leadership for complex large-molecule bioanalytical method development and serve as Primary Investigator on scientific client studies. Collaborate with clients and cross-functional teams to deliver scientifically rigorous solutions supporting drug development programs.
What You'll Be Doing
- Serve as Primary Investigator on scientific client studies, conducting laboratory work and communicating 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
- Provide meaningful data analysis and interpretation, 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, equipment standards, and compliance with applicable SOPs, regulatory requirements, and good documentation practices
What We Are Looking For
- Ph.D. in Chemistry, Analytical Chemistry, Biochemistry, Chemical Biology, Biology, or a related field preferred; peer-reviewed scientific publications in a relevant field preferred
- Master's degree in a science field plus 8+ years of experience with equivalent combination of education, training and experience in a bioanalytical laboratory environment
- Experience working with antibodies, antibody-drug conjugates, and oligonucleotide conjugates with payloads such as ASOs, PMOs, and siRNA is a plus
- Experience with analytical techniques such as mass spectrometry, CE-SDS, SDS-PAGE, BCA, SEC-HPLC, and UV-visible spectroscopy is a plus
- Experience evaluating the stability, potency, efficacy, and purity of therapeutic candidates used in in vitro and in vivo studies is a plus
- 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 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 while maintaining 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
Requirements
- Ph.D. in Chemistry, Analytical Chemistry, Biochemistry, Chemical Biology, Biology, or a related field preferred
- Master's degree in a science field plus 8+ years of 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 while maintaining 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
- Experience working with antibodies, antibody-drug conjugates, and oligonucleotide conjugates with payloads such as ASOs, PMOs, and siRNA is a plus
- Experience with analytical techniques such as mass spectrometry, CE-SDS, SDS-PAGE, BCA, SEC-HPLC, and UV-visible spectroscopy is a plus
- Experience evaluating the stability, potency, efficacy, and purity of therapeutic candidates used in in vitro and in vivo studies is a plus
Benefits
- Health & Welfare Benefits
- Incentive Plans
- Bonuses
Company overview
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Headquartered in Durham, North Carolina, the company operates in over 100 countries with approximately 86,000 employees worldwide. IQVIA specializes in creating intelligent connections across all aspects of healthcare through its proprietary IQVIA Connected Intelligence platform, which combines analytics, transformative technology, big data resources, and extensive domain expertise. The company's comprehensive portfolio includes clinical trial management, real-world evidence generation, commercial insights, and regulatory compliance services. IQVIA serves a diverse client base including pharmaceutical manufacturers, biotechnology companies, medical device firms, government agencies, and healthcare providers. With its Healthcare-grade AI capabilities and extensive global data assets, IQVIA accelerates the development and commercialization of innovative medical treatments while improving healthcare outcomes for patients globally. The company is publicly traded on the New York Stock Exchange under the ticker symbol IQV.