Scientific Writer II

Inotiv

2d•Hybrid

About The Position

The Scientific Writer II partners 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 that help our clients make informed decisions about their drug discovery programs. The individual in this role will work across sites with scientific staff and clients to ensure the accuracy, consistency, and professional appearance of all documents while adhering to templates, standards, and project timelines. Other responsibilities include performing statistical analysis using GraphPad Prism and/or R, developing and maintaining templates to improve workflows and increase efficiency, and assist in formatting a variety of papers, data packages, and other deliverables. ESSENTIAL DUTIES AND RESPONSIBILITIES 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 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 Sense of urgency to ensure that internal and external deadlines are met Detail-oriented and capable of producing consistent, error-free, quality deliverables Maintain thorough knowledge of facility SOPs, policies, study protocols, etc. Excellent organizational, communication, time management, and interpersonal skills in a cross-functional team General understanding of relevant regulations (e.g., GLP and GCP) Perform other duties as assigned

Requirements

Understanding of in vivo models of multi-system rodent physiology, immunology, neuroscience, histopathology, and in vitro analyses of pathobiology and disease biomarkers (molecular pharmacology and toxicology)
Ability to work independently as well as collaboratively with others across different company sites to ensure document accuracy, consistency, and professional appearance
Proficient in Microsoft Office, Adobe Acrobat, GraphPad Prism, and R
Follow all SOPs and other applicable laboratory or company policies and procedures
Interact with clients, other employees, and the community in a professional manner
Ability to adhere to all company policies, safety regulations and procedures
Maintain confidential information
Demonstrate Inotiv Core Values and adhere to Code of Conduct
Master's degree or higher in a related discipline (Physiology, Pharmacology, Immunology, etc)
At least 2 years of experience in pre-clinical in vivo models of disease
Any equivalent combination of education and experience

Nice To Haves

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

Responsibilities

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 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
Sense of urgency to ensure that internal and external deadlines are met
Detail-oriented and capable of producing consistent, error-free, quality deliverables
Maintain thorough knowledge of facility SOPs, policies, study protocols, etc.
Excellent organizational, communication, time management, and interpersonal skills in a cross-functional team
General understanding of relevant regulations (e.g., GLP and GCP)
Perform other duties as assigned