GLP Toxicology Reports Coordinator II

BAS EVANSVILLE INC; Evansville (IN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

401K

Paid time off

Disability insurance

Job summary

Inotiv in Evansville, IN seeks a Quality Control and Reports Coordinator II to compile data into comprehensive Toxicology Reports with tables and appendices. The role ensures accuracy, consistency, and professional presentation, and includes GLP/Non-GLP draft and final report preparation.

The position requires familiarity with CTD tables, data review, and collaboration with Study Directors and QA staff. Strong attention to detail and adherence to SOPs are essential.

Qualifications

• Preferred Education and Experience Associate’s Degree or higher in related sciences and/or at least 2 – 4 years’ experience in research as a Laboratory Animal Technician or Quality Assurance/Quality Control

Responsibilities

• Compile and generate Toxicology Reports with appropriate Tables, Appendices and Contributor Reports
• Review Clinical Pathology Data and CTD Tables for accuracy
• Prepare GLP and non-GLP Draft and Final Reports
• Ensure reports are accurate, consistent and professional
• Collaborate with Study Directors, QA Auditors and other personnel
• Archive study specimens and final reports
• Perform QA checks on data packs and PDFs
• Adhere to SOPs, protocols/amendments, and data integrity requirements

Skills

GLP compliance

SOP adherence

Data QA

Toxicology reports

CTD tables

Word/Excel/PDF

Education

Associate degree or higher in related sciences

Tools

Provantis

LIMS

Master Control

PDS

Ascentos

MS Access

Job description

Inotiv in Evansville, IN seeks a Quality Control and Reports Coordinator II to compile data into comprehensive Toxicology Reports with tables and appendices. The role ensures accuracy, consistency, and professional presentation, and includes GLP/Non-GLP draft and final report preparation.

The position requires familiarity with CTD tables, data review, and collaboration with Study Directors and QA staff. Strong attention to detail and adherence to SOPs are essential.