обновлено 8 дней назад
Scientist, Method Development - Ligand Binding Assays
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Scientist, Method Development - Ligand Binding Assays (Ligand Binding Bioanalytical Sciences): Developing ligand binding assays for the rapid and accurate analysis of proteins, peptides, and antibodies in biological matrices with an accent on immunoassay development, regulated bioanalytical studies, and assay validation. Focus on troubleshooting assay performance, interpreting data, evaluating new technologies, and providing technical leadership across study teams.
Location: Lincoln, Nebraska, United States; full-time onsite at the Lincoln facility
Company
conducts clinical research and translational medicine to help advance drug development.
What you will do
- Develop ligand binding assays using state-of-the-art technologies to analyze proteins, peptides, and antibodies in biological matrices.
- Perform pharmacokinetic, pharmacodynamic, biomarker, and anti-drug antibody assays under regulatory and quality systems.
- Analyze and interpret data, prepare summary tables, troubleshoot assay performance, and peer-review raw data.
- Develop bioanalytical methods by applying scientific theories, techniques, and regulatory requirements.
- Provide technical guidance to study teams and support innovation, change management, and evaluation of new technologies.
- Author scientific manuscripts, present research at conferences, and provide technical expertise during client interactions.
Requirements
- Bachelor’s degree in Biochemistry, Chemistry, or Biology; an advanced degree is preferred.
- 5+ years of related scientific experience preferred, with proven proficiency in immunoassay development.
- Hands-on experience in at least one area: pharmacokinetics, pharmacodynamics/biomarkers, or anti-drug antibody assay development.
- Understanding of FDA and ICH guidelines for method validation and sample analysis.
- Experience with ligand binding techniques such as ELISA, MSD, Gyrolab, or AlphaLISA.
- Strong technical writing, presentation, problem-solving, teamwork, and multitasking skills.
Nice to have
- Experience in a CRO or industry environment.
- Experience working in a regulated GLP-compliant environment.
- Experience using Watson LIMS.
Culture & Benefits
- Work in a collaborative, cross-functional scientific environment.
- Values include integrity, trust, teamwork, and respect.
- Opportunity to contribute to innovative clinical research and drug development.
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