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About the Role
ICON is a global healthcare intelligence and clinical research organisation focused on accelerating the delivery of new medicines and treatments to patients. We are a values-driven organisation committed to integrity, collaboration, agility, and inclusion.
Responsibilities
- Operate independently, make decisions, and project credibility.
- Identify key situation elements, data gaps, and inconsistencies, making rational judgments.
- Embrace and contribute to process improvement to streamline operations and meet client needs.
- Deliver high-quality standards, acting proactively and responsively to customer needs, potentially including overtime and weekend work.
- Conduct day-to-day activities to maintain the bioanalytical laboratory, including independently conducting validated assays on biological samples.
- Develop, qualify, and validate immunological, biochemical, and cell-based methods following GXP guidelines.
- Support data input into laboratory information management systems, documenting reagent inventory.
- Prepare reagents, buffers, solutions, and solvents according to SOPs and instructions.
- Train on, employ, and maintain routine operation, maintenance, and theory of instrumentation and software systems.
- Manage and keep current all training requirements.
- Follow SOPs and compliance regulations for safety, documentation, and scientific responsibility.
- Review and transform results, comparing data against method acceptance criteria and other relevant documents.
- Analyze data and interpret results, developing competency for independent delivery with input from senior staff.
- Contribute ideas for improving laboratory techniques, protocols, processes, and equipment.
- Make detailed observations of experiments, record data, maintain organized documentation, and perform peer review.
- Make and document scientific observations, identify, and independently solve problems in experimental designs.
- Provide timely review of calibration/maintenance, reconstitution, and protein processing data and notebook documentation.
- Keep management informed of study status, technical problems, and issues impacting the laboratory.
- Initiate and complete assigned work, assisting in meeting project and study goals.
- Advise and support junior scientists and management on deviations affecting data quality, accuracy, and usefulness.
- Document results, perform statistical analyses, and identify repeat or next-tier analysis needs.
- Interpret data to solve practical problems, isolate variables, troubleshoot assays, and propose CAPA.
- Read, analyze, interpret, and write scientific and technical documents.
- Serve as a technical subject matter expert, SOP owner, and qualified trainer on laboratory procedures.
- Perform statistical analysis and interpretation of data.
- Interface effectively with colleagues, managers, project leaders, sponsors, and at scientific meetings.
- Present unsolicited ideas for process improvement and foster continuous innovation.
- Interact with colleagues to ensure project timelines are met.
- Collaborate effectively with project members, adhering to priorities, checkpoints, and timelines.
- Design, direct, and participate in equipment and software validations/calibrations/maintenance.
- Plan daily, weekly, and monthly activities based on supervisor-established goals and timelines.
- Participate in internal seminars and scientific meetings for professional development and knowledge sharing.
- Determine repeat dilutions as applicable.
Requirements
- Associate’s degree in a science-related field and prior directly relevant experience will be considered.
Skills
- Immunological methods
- Biochemical methods
- Cell-based methods
- Laboratory information management systems
- Reagent preparation
- Instrumentation and software systems operation
- Compliance regulations
- Data analysis
- Statistical analysis
- Scientific documentation
- Troubleshooting
- Process improvement
- Collaboration
Location
- Onsite, Whitesboro, New York
Work Type
- Full-Time
- Onsite
Experience Level
- Scientist II
Education Level
- Associate’s degree in science related field
Salary/Compensations
- $57,800-$69,370
- $56,704.00-$70,880.00
Benefits
- Competitive salary packages
- Annual bonuses
- Health-related benefits
- Competitive retirement plans
- Life assurance
- Health and wellbeing programmes
- Medical, dental, and vision coverage
- Retirement and pension plans
- Disability coverage
- Employee assistance programmes
- Wellbeing resources
- Learning and development opportunities
- Structured training
- Career pathways
About the Company
- ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
- At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
- Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
- We’re driven by our vision and need talented people who share it.
- ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Equal Opportunity
- ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
- 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.