Celerion · 9 hours ago
Scientist, Method Development - Ligand Binding
Lincoln, NE
Full-time
Onsite
Senior Level
5+ years expCelerion is committed to swift, exceptional clinical research through translational medicine. They are seeking a Scientist to join their Ligand Binding Assay Development team, providing scientific expertise and method development skills to innovate and manage change in Ligand Binding Bioanalytical Sciences.
Health CarePharmaceutical
Responsibilities
Undertake original and innovative research and techniques that include developing ligand binding assays utilizing state-of-the-art technologies for the rapid and accurate analysis of protein/peptides/ antibodies in biological matrices
Perform assays (pharmacokinetics (PK), pharmacodynamics PD)/biomarkers, ADA) according to regulatory and quality systems
Analyze and interpret data, generate summary tables, and troubleshoot assay performance, as well as peer‑review raw data for accuracy and completeness
Work effectively within a team and across teams to meet objectives under time constraints
Support the associate director in achieving challenging business objectives for the method development team. Includes innovation, change management, evaluation of new technology, and growth in market share, revenue, profit, and customer loyalty
Develop methods by applying and interpreting scientific theories, concepts, techniques, and regulatory requirements in bioanalytical studies
Provide technical/scientific guidance and leadership to study teams, as well as other areas of the company to ensure project completion in a timely manner
Author scientific manuscripts for publication in peer‑reviewed journals and present research findings through posters and oral presentations at scientific conferences
Participate and provide technical expertise during client calls and visits
Qualification
Required
Minimum of a Bachelor's degree in Biochemistry, Chemistry or Biology required
5+ years of related scientific experience preferred, CRO/industry experience is a plus
The candidate must have proven proficiency in immunoassay development and be capable of working on multiple projects simultaneously
Strong hands-on experience in at least one of the following pharmacokinetics (PK), pharmacodynamics (PD)/biomarkers, ADA assay development
Understanding of FDA and ICH guidelines in method validation and sample analysis
Excellent verbal and technical writing skills and be capable of presenting to an audience of researchers from a variety of disciplines
Ability to work well with a team and with staff in other locations effectively
Preferred
An advanced degree is preferred
Prior experience working in a regulated GLP-compliant environment is preferred
Experience in one or more immunoassay techniques (Ligand Binding assay: ELISA, MSD, Gyrolab, AlphaLISA)
Experience using Watson LIMS is preferred
Company
Celerion
Celerion, a leader in early clinical research, delivers Applied Translational Medicine.
1001-5000 employees
H1B Sponsorship
Celerion has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (5)
2024 (7)
2023 (5)
2022 (3)
2021 (6)
2020 (5)
Funding
Current Stage
Late StageTotal Funding
unknown2022-11-03Acquired
2010-01-01Seed
Leadership Team
Susan C. Thornton
President and CEO
JoAnne Rosal
Chief Financial Officer
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