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Research Associate, Research Scientist, Clinical Research

Job in Deerfield, Lake County, Illinois, 60063, USA
Listing for: eTeam
Full Time position
Listed on 2026-09-15
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research
Salary/Wage Range or Industry Benchmark: 70000 - 100000 USD Yearly USD 70000.00 100000.00 YEAR
Job Description & How to Apply Below

Title:

Research Associate III

Location:

- Deerfield, IL

Duration: 12 Months

Description:

Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance. Display moderate technical understanding of related disciplines such as pH, temperature controlled reactions, and chemical reactions. Conduct routine/non-routine research and design experiments with minimal assistance. Essential

Duties and Responsibilities:

The incumbent will perform other duties assigned.

  • Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not. Provide some analysis/redesign of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility.
  • Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines. Identify existing alternative methods and technologies for improving existing or new products/processes.
  • Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
  • Manufacturability/Scale Up of biomaterials
    - Transfer from lab scale experiements to manufacturing production.
  • Contribute to technical feasibility analysis of complex research and design concepts.
  • Monitor budgets and/or activity schedules of external testing (communication, shipment, analysis of results and documentation).
  • In addition to having an in-depth knowledge and understanding of GxP and related regulations and guidance, is able to provide expert insights into such regulations so as to facilitate efficient product registration and/or is an active participant in the generation, review, adoption and interpretation of such regulations.
  • Demonstrate ability to apply technical theories and principles to projects within area of expertise for non-routine tasks. Analyze and determine best solutions to non-routine experimental design or research problems with minimal assistance. Accurately assess results for validity and conformance to specifications.
  • Qualifications:

    To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. The position requires relevant laboratory skills, writing skills, and computer skills plus teamwork/interpersonal skills.

    Education and/or

    Experience:

    Bachelor's Degree in a scientific discipline with at least 3-6 years lab experience or MS with at least 1-2 years of experience. Research lab experience may include research in GMP/QSR environment, cross-functional teamwork, and independent experimentation in method development and validation.

    An Ideal Candidate would have experience with:
    • Knowledge/experience with lyophilization
    • Knowledge/experience with Class 2/ 510k/ PMA FDA approved medical devices
    • Medical Device Product development experience
    Position Requirements
    10+ Years work experience
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