Toxicology Reports Lead: QC & Data Coordination

Inotiv, Inc.; Evansville (IN); Hybrid; USD 55,000 - 75,000; Full time

Job summary

Inotiv in Evansville, IN is seeking a Quality Control and Reports Coordinator II to compile and generate Toxicology Reports, including large data tables, appendices, and contributor reports. The role ensures accuracy, consistency, and professional presentation of reports written under GLP/Non-GLP guidelines.

Responsibilities include data package preparation, draft and final reports, review of clinical pathology data and CTD tables, and coordination with study directors and QA auditors to

Qualifications

• Associate’s Degree or higher in related sciences; 2–4 years’ research QA/QC experience.
• Knowledge of GLP compliance and data reporting preferred.

Responsibilities

• Understand, apply, and maintain adherence to GLP regulations, SOPs and Study Protocols/Amendments.
• Generate Non-GLP or GLP Main Toxicology Report Word Document, following templates and standards.
• Incorporate data into PDF documents and reports.
• Collaborate with Study Directors, QA Auditors, Report Writers, and third parties to prepare audited drafts and final reports.
• Confirm disposition of study specimens at finalization and perform archiving.
• Review Clinical Pathology Data Tables for accuracy and compliance to protocols.
• Review CTD Tables upon completion by the Study Director or assigned individual.
• Review data pack PDFs not yet reviewed or quality checked.
• Perform other duties as assigned by Supervisor.

Skills

Attention to detail

Strong organizational skills

Accurate documentation

Data review

Professional communication

Education

Associate’s Degree or higher in related sciences

Tools

Microsoft Word

Microsoft Excel

Adobe PDF

LIMS

Provantis

Job description

Inotiv in Evansville, IN is seeking a Quality Control and Reports Coordinator II to compile and generate Toxicology Reports, including large data tables, appendices, and contributor reports. The role ensures accuracy, consistency, and professional presentation of reports written under GLP/Non-GLP guidelines.

Responsibilities include data package preparation, draft and final reports, review of clinical pathology data and CTD tables, and coordination with study directors and QA auditors to