Associate Principal Scientist, Large Molecule Bioanalytical
IQVIA
Summary
Provide technical leadership for complex large-molecule bioanalytical method development and laboratory 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 laboratory 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 client studies, conduct laboratory work, and communicate study progress and results
- Design and execute complex bioanalytical method development experiments
- Evaluate and implement new methods, technologies, and instrumentation for client programs
- Prepare technical reports, study proposals, and protocols, including documentation that may support FDA submissions
- Lead multiple complex technical projects and guide or mentor junior scientific staff
- Analyze and interpret experimental findings, including statistical analysis, in accordance with laboratory standards
- Maintain laboratory notebooks, equipment, and study documentation in compliance with applicable regulatory standards, SOPs, and good documentation practices
- Collaborate across functions to deliver studies, deploy methods, and provide project updates to team leads and project managers
What We Are Looking For
- Master's degree in a science field
- 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 with antibodies, antibody-drug conjugates, or oligonucleotide conjugates containing payloads such as ASOs, PMOs, or siRNA
- Experience with large-molecule bioanalytical techniques such as 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 or in vivo studies
- Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role
- Demonstrated ability to independently manage multiple complex projects, priorities, and experimental deliverables
- Strong scientific writing, presentation, data interpretation, and client communication skills
- Ability to collaborate effectively across departments and contribute to multidisciplinary scientific discussions
- Advanced proficiency with Microsoft Excel, including statistical analysis, as well as PowerPoint, Word, and instrument-supporting software
- Working knowledge of applicable laboratory regulatory requirements, SOPs, and good documentation practices
- Demonstrated everyday leadership, mentoring, organization, interpersonal effectiveness, and time management skills
Requirements
- Master's degree in a science field
- 8+ years of experience in a bioanalytical laboratory environment
- Experience with antibodies, antibody-drug conjugates, or oligonucleotide conjugates containing payloads such as ASOs, PMOs, or siRNA
- Experience with large-molecule bioanalytical techniques such as 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 or in vivo studies
- Demonstrated ability to independently manage multiple complex projects, priorities, and experimental deliverables
- Strong scientific writing, presentation, data interpretation, and client communication skills
- Ability to collaborate effectively across departments and contribute to multidisciplinary scientific discussions
- Advanced proficiency with Microsoft Excel, including statistical analysis, as well as PowerPoint, Word, and instrument-supporting software
- Working knowledge of applicable laboratory regulatory requirements, SOPs, and good documentation practices
- Demonstrated everyday leadership, mentoring, organization, interpersonal effectiveness, and time management skills
Benefits
- Health and 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.