Scientist III
ICON plc
Summary
We are seeking candidates with a Bachelors in Biology, Chemistry, or Biotechnology and the ability to work in a fast paced collaborative environment. Familiarization with basic laboratory operations is preferred. Knowledge of binding assay formats and platforms, effective communication skills, attention to detail, and the ability to organize and prioritize work is required.
Job description
The Role: 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 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 overtime and weekend work at times.
- Travel (approximately 0%) domestic and/or international.
- Responsible to complete the day-to-day activities required to maintain the bioanalytical laboratory including responsibility for independently conducting validated assays on biological samples from pre-clinical and clinical trials for pharmaceutical and biotechnology projects under general supervision.
- 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.
- Prepares reagents, buffers, solutions and solvents in accordance with SOPs, methods and/or Sponsor instructions.
- Trains on, employs and maintains routine operation, maintenance and theory of instrumentation and software systems.
- Manages and keeps current all training requirements.
- Follows SOPs and relevant compliance regulations in regards to safety procedures, documentation, and scientific responsibility.
- Responsible for review and transformation/regression of results and data comparison against method acceptance criteria, methodology and other relevant direction documents.
- Analyzes data and interprets results with input from senior staff but with expectation to develop increasing competency for independent delivery.
- Contributes ideas and suggestions to improve standard laboratory techniques, protocols, processes and equipment.
- Makes detailed observations of experiments; record experimental data and maintains accurate and highly organized laboratory documentation including summaries; as well as performs peer review of peer records to create timely, accurate, legible, error-free lab records.
- Must make and document scientific observations and identify and solve problems in experimental designs with decreasing input from senior staff.
- Keeps managers and Project Leaders informed of study status, technical problems and other issues which impact the laboratory.
- Responsible for initiation and timely completion of work assigned and assists in meeting project and study goals.
- Advises the laboratory managers and Project Leaders of any deviations or factors that may affect quality, accuracy and usefulness of the data.
- To undertake other reasonably related duties as may be assigned from time to time.
- Effectively interfaces with other Scientists, Managers, Project Leaders, other members of the bioanalytical team, Sponsors and at scientific meetings.
What you need
We are seeking candidates with a Bachelors in Biology, Chemistry, or Biotechnology and the ability to work in a fast paced collaborative environment. Familiarization with basic laboratory operations is preferred. Knowledge of binding assay formats and platforms, effective communication skills, attention to detail, and the ability to organize and prioritize work is required.
Requirements
- Bachelors in Biology, Chemistry, or Biotechnology
- Ability to work in a fast paced collaborative environment
- Knowledge of binding assay formats and platforms
- Effective communication skills
- Attention to detail
- Ability to organize and prioritize work
- Familiarization with basic laboratory operations (preferred)
Benefits
- Competitive Base Salary
- Performance-Related Incentives
- Medical, Dental & Vision
- Retirement and Pension Plans
- Life Assurance
- Disability Coverage
- Employee Assistance Programmes
- Wellbeing Resources
- Learning and Development Opportunities
Company overview
ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.