Clinical Bench Scientist

Integrated Resources Inc.; Pearl River (NY); On-site; USD 60,000 - 85,000; Full time

Job summary

A prestigious staffing firm seeks an analyst to participate in the development of diagnostic assays for vaccines. This role involves collaboration, lab safety, data analysis, and requires relevant educational background in biology, immunology or microbiology. Successful candidates will have technical proficiency and experience in laboratory settings.

Qualifications

• Bachelor's degree required, 2 years relevant experience or a Master's degree.
• Laboratory experience in biology, immunology or microbiology is essential.

Responsibilities

• Generate and characterize reagents for assay development and qualification.
• Provide critical data review for clinical and non-clinical projects.
• Assist in updating documents and maintaining lab safety compliance.

Skills

Laboratory experience in biology

Immunology knowledge

Microbiology knowledge

Proficiency in Word

Proficiency in Excel

Proficiency in PowerPoint

Scientific software knowledge

Knowledge of Luminex technology

Education

Bachelor’s degree

Master’s degree

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

The position requires analyst participation in development and qualification of diagnostic ligand-binding assays for candidate and post-market vaccines in support of various programs.

Responsibilities:

· Generation and characterization of reagents, performance of experiments for development and qualification of assays, assay throughput for the pre-clinical studies and writing related procedures and reports.

· As an integral member of the dynamic team, the incumbent must have a strong work ethic and be highly collaborative with the other group members.

· All of the above includes practicing laboratory safety at all times and efforts toward GLP compliance.

· Perform all aspects of to support assay development and clinical testing.

· Provide critical data review of clinical and non-clinical data. Collect, collate and analyze data on a per project basis to support troubleshooting, qualification and other lab projects.

· Perform assays to support critical assay reagent testing, assay development/ troubleshooting.

· Assist in ordering supplies from internal inventory and order/prepare reagents/supplies necessary for assay work.

· Assist in updating and writing documents associated with assays, including information/data archiving, SOPs and status reports.

· Satisfactorily completes all GLP and safety training in conformance with Departmental requirements.

· Attend Power2Learn, corporate, and departmental training, as available.

· Must meet Vaccine Research Medical Surveillance requirements

Qualifications

Education & Experience:

Bachelor’s degree and 2 years relevant experience, or a Master’s degree.

Technical Skills Requirements:

Laboratory experience in a biology, immunology and/or microbiology.

Knowledge of Luminex technology is a plus.

The incumbent will be trained on required Policies, Practices, and Procedures needed to support work responsibilities.

Proficiency in theuse of Word, Excel, PowerPoint and relevant scientific software is desirable