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Support Scientist I, Bioanalytical Chemistry at Charles River Laboratories Ashland, KY

Job in Ashland, Boyd County, Kentucky, 41114, USA
Listing for: Itlearn360
Full Time position
Listed on 2026-07-30
Job specializations:
  • Research/Development
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 22 - 24 USD Hourly USD 22.00 24.00 HOUR
Job Description & How to Apply Below

Support Scientist I, Bioanalytical Chemistry at Charles River Laboratories in Ashland, KY.

Job Summary

We are seeking a Support Scientist I (Bioanalytical Chemistry) for our Safety Assessment Group site located in Ashland, Ohio. This entry level position involves developing skills to understand assigned department study designs. You will acquire basic knowledge of data collection systems and an introduction to protocol development, regulatory compliance and internal systems used in study conduct. Excellent verbal and written communication skills are required.

You will be trained to become proficient in direct communication with clients and to develop training in quantitative data analysis review.

Essential Duties and Responsibilities
  • Create/customize planning tools to facilitate prioritization of daily activities.
  • Maintain department, study, and inventory trackers in support of Project Scientist.
  • Interact regularly with sponsors: send amendments and regulatory forms for signature, respond to sponsor‑requests for information and tables, and assist with sponsor on‑site visits.
  • With guidance, write initial protocol drafts and, upon study director approval, distribute draft protocols for internal and/or sponsor review and coordinate the amendment/revision process.
  • Facilitate signature/approval process for protocol, amendments and other required forms.
  • Tabulate study data and schedule data review meetings.
  • Assist in creation/generation of special tables for sponsors as needed.
  • Assemble report (text and data tables) for senior scientific review, QA audits and final report compilation.
  • Ensure all study books are corrected appropriately and that documentation is GLP compliant prior to submission to QA.
  • Assist in documentation of deviations from the protocol or SOP and assist in drafting new or study‑specific SOPs.
  • Efficiently perform, review, and document all study data, procedures, materials, and results in compliance with applicable regulatory standards, SOPs and methods/protocols.
  • Complete administrative tasks such as filing and placing orders as needed.
  • Develop effective communication skills through informal discussions with peers, supervisor, team and sponsor/SDs.
  • Develop critical thinking, troubleshooting and time management skills aligned with operational needs.
  • Perform all other related duties as assigned.
Pay Range

Pay range for this position is $22–24 USD per hour. Starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location. This is a hybrid role.

Job Qualifications
  • Education:

    High School diploma or GED preferred. Associate's degree (A.A./A.S.) or equivalent from two‑year college recommended. Bachelor's degree (B.A./B.S.) or equivalent in a related discipline strongly recommended.
  • Experience:

    Zero to two years related experience in biology, chemistry/pharmacy or similar lab environment. GLP experience preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute.
  • Certification/Licensure:
    None.
  • Other:
    • Analytical thinking skills and a good understanding of scientific processes.
    • Strong organizational skills and attention to detail.
    • Computer skills including MS Office software and database management.
    • Knowledge of GLP regulations and understanding of routine study design and protocols.
Comments

This position requires overtime, weekend, holiday, and/or after‑hours shift coverage as needed.

Benefits
  • Bonus/incentives based on performance
  • 401(k)
  • Paid time off
  • Stock purchase program
  • Health and wellness coverage
  • Employee and family wellbeing support programs
  • Work‑life balance flexibility
Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e‑mail message to  This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

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