About this role
Role Overview
- partner with study directors, principal investigators, and other scientific staff to generate high-quality figures, tables, protocols, and technical reports from pre-clinical drug discovery, pharmacology, and toxicology study data
- work across sites with scientific staff to ensure the accuracy, consistency, and professional appearance of all documents while adhering to templates, standards, and project timelines
- develop and maintain templates to improve workflows and increase efficiency
- assist in formatting a variety of data packages and other deliverables
- partner with scientific staff to produce accurate and concise reports and data packages
- setup spreadsheets or other documentation as directed by scientific staff to allow for accurate and efficient data entry
- create, edit, and format tables and figures from applicable software programs
- analyze and interpret data across a range of therapeutic areas
- review reports and other documents for spelling, grammar, clarity, and conformance with applicable templates
- work with other departments, groups, or teams as necessary to create and issue reports, amendments, and other required deliverables
- convert deliverables to PDF and format them in compliance with applicable FDA guidelines and Inotiv style guides and templates
- maintain thorough knowledge of facility SOPs, policies, study protocols, etc.
Requirements
- Bachelor’s degree or higher in a related discipline (Physiology, Pharmacology, Immunology, etc); Master’s preferred
- 2 years of experience in pre-clinical in vivo models of disease preferred
- Any equivalent combination of education and experience
- Past pre-clinical, scientific, and/or technical writing experience preferred
- Equivalent combination of related education and required work experience will be considered with Management approval
Benefits
- health and dental coverage
- short
- and long-term disability
- paid time off
- paid parental leave
- 401K
- and more!