Scientific Writer

The Scientific Writer 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.

LOGISTICS

• This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and / or years of experience. The salary range for this role is $70,000 - $90,000 and can adjust along with the level of the role to match the person's relevant experience and / or education level.

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

SKILLS AND ABILITIES

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

MINIMUM EDUCATION AND EXPERIENCE

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

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

WORKING CONDITIONS

Work is normally performed in a typical interior office

Option for a hybrid schedule

Prolonged periods of sitting at a desk and working on a computer

Teamwork setting

Consistent written and verbal communication

#LI-Hybrid #LI-OF1

Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.

Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!

Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.