Support Scientist I, Bioanalytical Chemistry

Charles River Laboratories•Ashland, OH

64d•$22 - $24•Hybrid

About The Position

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary We are seeking a Support Scientist I (Bioanalytical Chemistry) for our Safety Assessment Group site located in Ashland, Ohio. Basic Summary: Entry level support scientist developing skills to understand assigned department study designs. Limited or basic knowledge of data collection systems. Introduction to protocol development, regulatory compliance and internal systems utilized in the conduct of a study. Excellent verbal and written communication skills. Train to become proficient in direct communication with clients. Develop training in quantitative data analysis review.

Requirements

Education: High School diploma or General Education Degree (G.E.D.) 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 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 for the specific education and experience listed above.
Certification/Licensure: None.
Other: This position requires analytical thinking skills and a good understanding of scientific processes. Strong organizational skills and attention to detail required, as are computer skills including MS Office software and database management. Knowledge of GLP regulations and understanding of routine study design and protocols.

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. Upon study director approval, distribute draft protocols for internal and/or sponsor review, and coordinate amendment/revision process.
With guidance, facilitate signature/approval process for protocol, amendments, and other required forms.
With guidance, tabulate study data and schedule data review meetings.
Assist in the creation/generate special tables for sponsors as needed.
With guidance, assemble report (text and data tables) for senior scientific review, QA audits, and final report compilation.
Ensure that 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 Standard Operating Procedures (SOP). 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.
Effectively 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 needs of operational areas.
Perform all other related duties as assigned.