Research & Development Clinical Scientist Jobs in USA, IL, Cary | Rose International Job

Rose International

Trout Valley, IL

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JOB DETAILS

SALARY

$40–$42 Per Hour

JOB TYPE

Temporary

SKILLS

Analysis Skills, Analytical Method Validation, Career Development, Chemistry, Clinical Research, Communication Skills, Cross-Functional, Data Analysis, Documentation, Emerging Technology, Fourier-Transform Infrared Spectroscopy (FTIR), GMP (Good Manufacturing Practices), Healthcare Quality, High Performance Liquid Chromatography (HPLC), Industry/Trade Analysis, Instrumentation, Laboratory Equipment, Laboratory Notebook, Laboratory Testing, Medical Affairs, Problem Solving Skills, Procedure Development, Product Development, Product Support, Quality Assurance Methodology, Regulations, Regulatory Requirements, Research & Development (R&D), Risk Analysis, Sample/Specimen Processing, Standard Operating Procedures (SOP), Team Player, Technical Writing, Test Data, Test Plan/Schedule, UV/VIS (Ultraviolet-Visible Spectroscopy)

LOCATION

Trout Valley, IL

POSTED

4 days ago

Required Education: Bachelor's degree in chemistry Required Experience/Skills: 6+ years of hands-on experience with analytical instrumentation, including HPLC, GC, FTIR, UV-Vis, and related laboratory equipment. 6+ years of experience developing, optimizing, and validating analytical methods. Demonstrated proficiency in operating analytical instruments and interpreting complex data. Excellent analytical, problem-solving, technical writing, and communication skills. Experience collaborating with cross-functional teams in a regulated environment. Ability to maintain detailed laboratory documentation and follow established procedures.Job Duties: Develop, optimize, and validate analytical methods using HPLC, GC, FTIR, UV-Vis, and other laboratory instrumentation. Perform sample preparation, testing, data analysis, and result interpretation. Maintain accurate documentation in laboratory notebooks and electronic systems. Collaborate with R&D, Regulatory Affairs, Quality, Medical Affairs, and Product Development teams to advance research initiatives. Follow, review, and draft SOPs, test methods, and GMP-compliant procedures. Provide scientific expertise and recommendations to support product claims, risk assessments, and clinical strategies. Interpret and apply clinical, scientific, and regulatory requirements to research activities and development projects. Work independently while exercising sound scientific judgment and decision-making with minimal supervision. Monitor industry trends, emerging technologies, and advancements in clinical research to identify opportunities for innovation. Ensure compliance with applicable regulatory, ethical, quality, and clinical research standards. **Only those lawfully authorized to work in the designated country associated with the position will be considered.** **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.** Benefits: For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay Equity: For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances. If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

About the Company

Rose International

Founded in 1993 by Sue Bhatia, Rose International is one of the nation's leading minority- and woman-owned providers of Staffing and Total Talent Solutions. We serve companies in all 50 states and employ thousands of people across the country.

COMPANY SIZE

2,500 to 4,999 employees

INDUSTRY

Staffing/Employment Agencies

WEBSITE

https://www.roseint.com/