Analytical Chemistry Research Scientist | GLP & Study Lead

Charles River; Reno (NV); On-site; USD 90,000 - 95,000; Full time

Job summary

Charles River is seeking an experienced Research Scientist (Analytical Chemistry) for our Safety Assessment site in Reno, NV. The role involves conducting preclinical and clinical studies, study direction under GLP, data interpretation and reporting, and ensuring regulatory compliance.

You will lead sponsor interactions and provide scientific guidance to staff. Ideal candidates have 3–5 years in CRO/academic/pharmaceutical settings, strong analytical skills (HPLC, SoloVPE, UV-Vis, CE, iCIEF),

Qualifications

• Bachelor's degree in a scientific field; MS or PhD preferred.
• 3–5 years of related CRO/academic/pharmaceutical experience.
• Expert in analytical techniques (HPLC, SoloVPE, UV-Vis, CE, iCIEF).
• Knowledge of GLP and regulatory study requirements.
• Strong written and verbal communication; able to manage multiple projects.

Responsibilities

• Conduct preclinical/clinical studies of basic to moderate complexity with study management and data reporting.
• Act as study director ensuring GLP compliance and study direction.
• Coordinate study planning with relevant departments.
• Generate protocols, amendments, and study reports.
• Review and present data; provide scientific guidance to staff.
• Interface with sponsors for study planning, scheduling, and proposals.

Skills

Analytical techniques

Study management

Regulatory compliance

Communication skills

MS Office (Excel/Word/PowerPoint)

Education

Bachelor's degree in science

MS/PhD preferred

Tools

HPLC

SoloVPE

UV-Vis

CE

iCIEF

Job description

Charles River is seeking an experienced Research Scientist (Analytical Chemistry) for our Safety Assessment site in Reno, NV. The role involves conducting preclinical and clinical studies, study direction under GLP, data interpretation and reporting, and ensuring regulatory compliance.

You will lead sponsor interactions and provide scientific guidance to staff. Ideal candidates have 3–5 years in CRO/academic/pharmaceutical settings, strong analytical skills (HPLC, SoloVPE, UV-Vis, CE, iCIEF),