Scientist Iii

4 weeks ago


New York, United States Icon plc Full time

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 Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Job Description: Scientist III;
- Recognize, exemplify and adhere to ICON's values which center around our commitment to People Clients and Performance.
- As a member of staff, the employee I expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Operates independently with a willingness to make decisions; projects credibility and makes a professional and positive impression on others; monitors progress and holds self and others accountable to contribution and quality.
- As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Delivers high quality standards and strives for excellence; acts in a proactive, flexible and responsive manner to customer needs which may necessitate weekend work at times.
- Work with clients to bring externally established assays and technologies in-house and/or transfer in-house assays externally as required.*
- Identify changes to scope of work and notify contracts of need for change order.*
- Review all data in accordance with direction documents and ensure results are documented accurately, completely and compliant with GLP/GCP regulations and SOPs.
- Assist Project Leaders and lab staff in proactively identifying possible/potential implications of unusual results. Assist as required in an investigation and report findings.*
- Develops, qualifies, and validates a variety of immunological, biochemical, and cell-based methods independently but with team interaction supporting preclinical and clinical studies following applicable GXP guidelines.*
- Generate high quality analytical results. Ensure smooth transfer of data to PI’s and participate in evaluation and interpretation of data*
- Analyzes data and interprets results with limited input from senior staff.*
- Prepare Bioanalytical method documents.
- Supports data input into laboratory information management systems including documenting receipt, entering and maintaining inventory of assay reagents, supplies and controls required for use in bioanalytical methods.
- Identifies the key elements of a situation and any gaps and inconsistencies in data. Makes rational judgements from available information and analysis.*
- Other duties as assigned.
- Travel (approximately



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