Principal Scientist

ICON plcLenexa, KS
Onsite

About The Position

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. Are you a scientist with expertise in method development? Take the next step in your career by joining ICON where you’ll advance groundbreaking clinical therapies by leading global client programs. We are excited to be seeking a new Principal Scientist at ICON in Lenexa, Kansas (KS). The Principal Scientist will lead and conduct scientific research aimed at advancing clinical trials and developing innovative therapies. You will manage sponsor programs, shape assay strategies, and provide expertise for new and complex modalities. We are seeking candidates with robust method development and knowledge in science for new biological modalities.

Requirements

  • Read, write and speak fluent English.
  • BS in a scientific discipline required.
  • 5 – 10 years of industry or academic laboratory experience supporting ligand-binding assays.
  • Demonstrated method development experience within the clinical or pharmaceutical industry with a track record of managing scientific projects.
  • Ligand binding assays
  • ELISA, ECLIA
  • PK, PD, and immunogenicity
  • Usage of relevant software (e.g. SoftMax Pro, Watson, or equivalent)

Nice To Haves

  • Advanced degree (MS or PhD), preferred.
  • Neutralizing antibody or Flow Cytometry experience is beneficial.
  • Presenter/Publisher in Regulated relevant field, nice to have.

Responsibilities

  • Responsible for method development and validation testing using complex ligand-binding analytical methods.
  • Oversee transfer of LBA methods for large molecules for further bioanalytical testing.
  • Designs and executes experiments for method development under supervision or independently depending on level.
  • Develops new scientific approaches to method development and communicates these to the global science team.
  • Mentor more junior scientists and advise operation on developed methods.
  • Reviews and approves data of other scientists.
  • Communicate with team members and management regarding project status, purpose, scheduling, problems, etc.
  • Communicate and/or participate in communication with clients regarding project status.
  • Maintain knowledge and skill in all techniques where you perform your work.
  • Provide scientific input to management and BD about new technology investments and lines of service.
  • Discusses scientific results with sponsors together with project manager.
  • Promotes ICON utilizing their scientific skills through scientific communication such as external publication of posters and journal articles.
  • Perform R&D projects.
  • Training of technicians on technical aspects.
  • Mentor and train staff on scientific topics.
  • Takes initiative in process development and SOP/WI writing.
  • Legible, logical and reproducible documentation of all experimentation.
  • Has a thorough understanding and complies with GLP and other appropriate regulations.
  • Develops rugged and economical assays.
  • Performs data review of other scientist’s work.
  • Provides key assay input to the validation and bioanalysis team(s) to ensure successful execution.
  • Assay troubleshooting.
  • May perform and document maintenance, troubleshooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel.

Benefits

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways
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