Date Posted: 06/01/2026
Hiring Organization: Rose International
Position Number: 502083
Industry: Medical Equipment & Supplies
Job Title: Research & Development Clinical Scientist
Job Location: Cary, IL, USA, 60013
Work Model: Onsite
Shift: 8am-5pm, Monday- Friday
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 22
Min Hourly Rate($): 40.00
Max Hourly Rate($): 42.00
Must Have Skills/Attributes: Clinical, GMP, HPLC, Laboratory, Research, Scientist
Experience Desired: Analytical lab experience with HPLC, GC, FTIR, and UV-Vis in a GMP environment (6-8 yrs); Analytical method development, validation, and troubleshooting experience. (6-8 yrs); Strong data analysis and technical documentation skills (6-8 yrs)
Required Minimum Education: Bachelor’s Degree
**C2C is not available**
Job Description
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.).
Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.
Diane, Consultant
Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.
David, Consultant
I believe the best thing that Rose HR has going for it is the incredible responsiveness. Everyone is very quick to reply to any concerns, and contacts the contracted employees very quickly and efficiently.
Kevin, Consultant
As a contractor, I have to say that Rose International was by far the best agency I have worked for.
Q'testdalir, Consultant
You are customer service oriented. No matter whether it was the Recruiter or someone in Human Resources/Payroll, you were responsive. That to me is key!
Tonya, Consultant
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