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.

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

Inotiv

Open Positions (1)