Celerion3mo ago

Scientist, Method Development - Ligand Binding

United States·LincolnFull-Timemid

OtherDevelopment

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Quick Summary

Overview

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Technical Tools

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Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!

Celerion is seeking a Scientist to join our Ligand Binding Assay Development team. The successful candidate will have strong problem-solving skills, scientific expertise and knowledge in Ligand Binding bioanalytical method development.

This full-time role is located at our Lincoln, NE facility.

As a Scientist, Method Development, you will provide scientific expertise and method development skills to the Ligand Binding Assay Development group at Celerion. A key component of the role is to provide innovation and change management required to remain on the cutting edge of Ligand Binding Bioanalytical Sciences.

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

Minimum of a Bachelor’s degree in Biochemistry, Chemistry or Biology required. An advanced degree is preferred.

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

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

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

Location & Eligibility

Where is the job

Lincoln, United States

On-site at the office

Who can apply

Listed under

United States

Listing Details

Posted: January 30, 2026
First seen: March 26, 2026
Last seen: May 14, 2026

Posting Health

Days active: 48
Repost count: 0
Trust Level: 31%
Scored at: May 14, 2026

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Celerion

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Celerion is a leading Clinical Research Organization focused on accelerating early phase drug development through innovative strategies and comprehensive research services.

Employees

3k+

Founded

2010

Domain

Jobs

External application · ~5 min on Celerion's site

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