Celerion

Global CRO for early-phase development

Director of Ligand Binding Assays

Biology & BiotechConfirmed live in the last 24 hours

Full-timeTempe, AZ, USANo salary listed

About the Job

Requirements

A Ph.D. or M.Sc. degree in biochemistry, immunology, pharmacology, analytical sciences, molecular biology, biotechnology, or a related scientific discipline, with significant relevant industry experience in regulated bioanalysis supporting nonclinical studies and clinical trials.
A minimum of approximately 12 years of relevant industry experience, including progressive leadership responsibility and change management within ligand binding or large-molecule bioanalysis.
Deep scientific understanding and practical experience with ligand binding assay principles, with strong experience in large-molecule pharmacokinetic, biomarker, and immunogenicity bioanalysis.
Working knowledge of applicable regulatory expectations and industry guidance governing regulated bioanalysis, including relevant FDA, EMA, ICH, and GLP/GCP expectations.
First-hand experience as a Study Director, Principal Investigator, Bioanalytical Project Manager, or equivalent role supporting regulated studies within a GLP/GCP-compliant environment.
Experience participating in or supporting sponsor audits and Health Authority regulatory inspections.
Demonstrated experience managing, developing, and leading scientific teams, preferably within a growing or changing laboratory environment, with the ability to develop talent, manage performance, and foster collaboration and knowledge sharing.
Demonstrated ability to translate business demand into staffing, equipment, technology, capacity, and financial plans.
Strong client-facing skills and the ability to explain complex scientific and regulatory concepts clearly to technical and non-technical audiences.
Experience supporting proposals, scientific presentations, bid defenses, and business development activities.
Knowledge of laboratory automation, data acquisition and analysis systems, electronic laboratory systems, and LIMS platforms such as Watson or equivalent systems.
Experience utilizing scientific software, data analysis systems, statistical tools, and emerging digital technologies.
Strong written and verbal communication skills and the ability to influence across functions and organizational levels.
Demonstrated ability to manage multiple priorities, resolve complex scientific and operational problems, and make sound decisions in a fast-paced environment.

Responsibilities

Provide leadership for the Ligand Binding Assay teams across Phoenix and Lincoln by building a high-performing, collaborative organization focused on scientific excellence, accountability, and continuous improvement.
Develop talent through coaching, performance management, and succession planning, while ensuring the laboratory has the people, resources, capacity, and technology needed to meet growth objectives.
Oversee operational performance to ensure revenue, quality, productivity, and client timelines are consistently achieved.
Serve as the senior scientific leader and subject matter expert for ligand binding bioanalysis, providing oversight for the development, validation, transfer, and execution of bioanalytical methods supporting biologics and other large-molecule therapeutics.
Ensure studies are scientifically sound, compliant with regulatory expectations, and aligned with client needs; drive innovation through new technologies, automation, and process improvements.
Ensure laboratory activities comply with GLP, GCP, EHS, and applicable regulatory requirements; maintain inspection readiness, support audits, promote right-first-time execution, and partner with Quality Assurance and operational teams to improve processes and quality systems.
Partner with Business Development and senior leadership to support growth initiatives, evaluate opportunities, and strengthen client relationships.
Serve as a scientific advisor during client interactions, capability presentations, and proposal development, delivering solutions that meet client objectives and support customer satisfaction, retention, and long-term business success.
Represent Celerion in the bioanalytical community through professional organizations, industry collaborations, conferences, and scientific publications.
Monitor emerging technologies, regulatory developments, and industry trends and use this knowledge to advance Celerion's capabilities, reputation, and competitive position.
Provide broader operational leadership at the Phoenix site through collaboration with Molecular & Cell-Based, Dose Formulation Analysis, and other functional groups.

Desired Qualifications

A strong external scientific profile, including participation in professional organizations, scientific meetings, industry working groups, publications, or presentations.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to get innovative medicines to market faster and help patients as quickly as possible. Our world-leading bioanalytical labs have been supporting pharmaceutical and biotech companies around the world for more than 50 years.

Due to steady and sustainable expansion, we are looking for a full-time Director of Ligand Binding Assays based on-site in Tempe, Arizona, USA. In this role you will play a crucial role in driving and leading the development and implementation of regulatory quality LBA methods to progress sponsor drug developments programs. This role will be instrumental in expanding our Phoenix bioanalytical capabilities while providing leadership oversight for LBA activities across multiple sites. If you are passionate about using your bioanalytical expertise and leadership to improve patient’s lives then we would love for you to join our dynamic team.

The Director of Ligand Binding Assays provides scientific, operational, and strategic leadership for Celerion's U.S. LBA organization, with primary responsibility for the growth and success of the Phoenix laboratory and leadership oversight of LBA activities in Lincoln, Nebraska. This role is responsible for building high-performing teams, driving scientific excellence, ensuring regulatory compliance, achieving business objectives, and delivering exceptional client service. The Director will partner closely with Bioanalytical Services leadership and cross-functional teams to support growth, innovation, and operational excellence. Additionally, this role provides broader operational leadership at the Phoenix site through collaboration with Molecular & Cell-Based (MCB), Dose Formulation Analysis (DFA), and other functional groups.

Leadership & Operations

Provide leadership for Celerion's Ligand Binding Assay teams across Phoenix and Lincoln by building a high-performing, collaborative organization focused on scientific excellence, accountability, and continuous improvement. This role is responsible for developing talent through coaching, performance management, and succession planning while ensuring the laboratory has the people, resources, capacity, and technology needed to meet growth objectives. The Director also oversees operational performance, ensuring revenue, quality, productivity, and client timelines are consistently achieved.

Scientific Leadership

Serve as the senior scientific leader and subject matter expert for ligand binding bioanalysis, providing oversight for the development, validation, transfer, and execution of bioanalytical methods supporting biologics and other large-molecule therapeutics. The Director will ensure studies are scientifically sound, compliant with regulatory expectations, and aligned with client needs while driving innovation through new technologies, automation, and process improvements.

Quality & Compliance

Lead a culture of quality and compliance by ensuring all laboratory activities are performed in accordance with GLP, GCP, EHS, and applicable regulatory requirements. The Director is accountable for maintaining inspection readiness, supporting audits, promoting right-first-time execution, and partnering with Quality Assurance and operational teams to continuously improve processes and quality systems.

Business & Client Engagement

Partner with Business Development and senior leadership to support growth initiatives, evaluate new opportunities, and strengthen client relationships. The Director serves as a scientific advisor during client interactions, capability presentations, and proposal development, helping to deliver solutions that meet client objectives while contributing to customer satisfaction, retention, and long-term business success.

Industry Leadership

Represent Celerion as a leader within the bioanalytical community by participating in professional organizations, industry collaborations, conferences, and scientific publications. The Director will stay informed on emerging technologies, regulatory developments, and industry trends, utilizing this knowledge to advance Celerion's capabilities, reputation, and competitive position in the marketplace.

Requirements

Ph.D. or M.Sc. degree in biochemistry, immunology, pharmacology, analytical sciences, molecular biology, biotechnology, or a related scientific discipline, with significant relevant industry experience in regulated bioanalysis supporting nonclinical studies and clinical trials.

A minimum of approximately 12 years relevant industry experience, including progressive leadership responsibility and change management within ligand binding or large molecule bioanalysis.

Deep scientific understanding and practical experience with ligand binding assay principles with strong experience with large molecule pharmacokinetic, biomarker and immunogenicity bioanalysis.

Working knowledge of applicable regulatory expectations and industry guidance governing regulated bioanalysis, including relevant FDA, EMA, ICH, and GLP/GCP expectations.

First-hand experience as a Study Director, Principal Investigator, Bioanalytical Project Manager or equivalent role supporting regulated studies within a GLP/GCP-compliant environment.

Experience participating in or supporting sponsor audits and Health Authority regulatory inspections.

Demonstrated experience managing, developing, and leading scientific teams, preferably within a growing or changing laboratory environment, with demonstrated ability to develop talent, manage performance, and foster collaboration and knowledge sharing.

Demonstrated ability to translate business demand into staffing, equipment, technology, capacity, and financial plans.

Strong client-facing skills with the ability to explain complex scientific and regulatory concepts clearly to both technical and non-technical audiences.

Experience supporting proposals, scientific presentations, bid defenses, and business development activities.

Knowledge of laboratory automation, data acquisition and analysis systems, electronic laboratory systems, and LIMS platforms such as Watson or equivalent systems.

Experience utilizing scientific software, data analysis systems, statistical tools, and emerging digital technologies.

Strong written and verbal communication skills and demonstrated ability to influence across functions and organizational levels.

Demonstrated ability to manage multiple priorities, resolve complex scientific and operational problems, and make sound decisions in a fast-paced environment.

A strong external scientific profile, including participation in professional organizations, scientific meetings, industry working groups, publications, or presentations, is preferred.

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

About the Company

Celerion

Global CRO for early-phase development

Celerion is a global contract research organization focused on early-phase drug development. It conducts contracted research across clinical trial design, feasibility studies, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, using High Resolution Mass Spectrometry-based metabolite profiling to inform decisions. Its advantage comes from over 40 years of experience, specialized metabolite profiling, and a global, integrated service model that accelerates development timelines. The goal is to help pharmaceutical and biotech clients bring safe and effective treatments to patients faster through rigorous, high-quality research.

Company size: 1,001-5,000
Company stage: Acquired
Total funding: Not listed
Headquarters: Lincoln, NE
Founded: 2010

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