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.

We are excited to be seeking a new Sr. Principal Scientist (Sr. Research Scientist) at ICON in Lenexa, Kansas (KS). The Sr. Principal Scientist (Sr. Research Scientist) will play a crucial role in designing, conducting, and analyzing complex clinical research studies.

You will leverage your expertise to drive innovative research initiatives, develop scientific protocols, and collaborate across departments to ensure the successful execution of clinical trials that advance new treatments and therapies.

A successful candidate will have advanced experience in ligand binding assays:

• ELISA, ECLIA
• PK, PD, and immunogenicity
• Usage of relevant software (e.g. SoftMax Pro, Watson)
• Neutralizing antibody (NAb)

What you'll be doing:

Method Development

• Independently designs and executes experiments for LBA method development.
• 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.
• Responsible for organized and effective communication with the internal team and management, and with clients regarding project status, scheduling, barriers, etc.

Scientific

• Provide scientific input to management and BD about new technology investments and lines of service.
• Drive new business by consulting with sponsors on assay requirements for new projects.
• Promotes ICON utilizing scientific skills through scientific communication such as external publication of posters and journal articles.
• Mentor and train staff on scientific topics.

Quality and Timely Work Execution

• Takes initiative in process development and SOP/WI writing.
• 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.

Sample Analysis and Assay Validation

• Provides key assay input to the validation and bioanalysis team(s) to ensure successful execution.
• Provide support to Laboratory Operations staff regarding assay quality, expected results, troubleshooting and data review.
• May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel.

Your Profile:

• PhD with applicable research in a relevant scientific field and 2+ years of CRO experience
• OR MS or BS in Science and 10+ years of experience in a relevant laboratory environment
• Extensive experience in clinical research design, data analysis, and interpretation, with a strong publication record.
• Presenter/Publisher in Regulated relevant field preferred.
• Strong analytical and problem-solving skills, with a commitment to scientific excellence.
• Excellent communication and leadership skills, with the ability to work effectively in cross-functional teams.

#LI-KM3

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply