Director, Ligand Binding Assays

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.

 

 

 

 

 

 

 

• 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.