📌 Core Information
🔹 Job Title: Scientific Writer II
🔹 Company: Inotiv
🔹 Location: St. Louis MO - Worthington, United States
🔹 Job Type: Full-Time, Hybrid
🔹 Category: Research Services
🔹 Date Posted: August 7, 2025
🔹 Experience Level: 2-5 years
🔹 Remote Status: On-site with hybrid option
🚀 Job Overview
Key aspects of this role include:
- Collaborating with scientific staff to generate high-quality figures, tables, protocols, and technical reports
- Ensuring document accuracy, consistency, and professional appearance while adhering to templates, standards, and project timelines
- Performing statistical analysis using GraphPad Prism and assisting in formatting various deliverables
- Working across sites with scientific staff and clients to maintain a sense of urgency and meet internal and external deadlines
ASSUMPTION: This role requires a strong attention to detail, excellent communication skills, and the ability to work independently and collaboratively with others across different company sites.
📋 Key Responsibilities
✅ 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
✅ 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 protocols, 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 protocols, 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.
✅ Perform other duties as assigned
ASSUMPTION: This role may require occasional overtime or working on weekends to meet project deadlines.
🎯 Required Qualifications
Education: Master's degree or higher in a related discipline (Physiology, Pharmacology, Immunology, etc.)
Experience: At least 2 years of experience in pre-clinical in vivo models of disease
Required Skills:
- 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, and GraphPad Prism
- 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
Preferred Skills:
- Past pre-clinical, scientific, and/or technical writing experience
ASSUMPTION: Candidates with equivalent combinations of education and experience may be considered with Management approval.
💰 Compensation & Benefits
Salary Range: $60,000 - $80,000 per year (based on experience and education level)
Benefits:
- Health and Dental Coverage
- Short- and Long-term Disability
- Paid Time Off
- Paid Parental Leave
- 401K
Working Hours: Full-time, typically 40 hours per week, with a hybrid schedule option
ASSUMPTION: The salary range provided is an estimate based on industry standards for this role, experience level, and location. Actual salary may vary based on individual qualifications and company discretion.
📌 Applicant Insights
🔍 Company Context
Industry: Inotiv operates in the Research Services industry, focusing on drug discovery and development solutions for clients worldwide.
Company Size: Inotiv has 1,001-5,000 employees, providing a mid-sized company environment with opportunities for growth and collaboration.
Founded: Inotiv was founded in 2019, with a history of providing world-class drug discovery and development solutions.
Company Description:
- Inotiv is a growing contemporary drug discovery and development company that plays to win in an industry rich with opportunity.
- The company focuses on delivering world-class drug discovery and development solutions that impact the health and well-being of people all over the world.
- Inotiv offers career opportunities for individuals at all phases of their careers, with a commitment to embracing research and science to make a difference in people's lives.
Company Specialties:
- Preclinical services
- Drug discovery
- Research models
- Regulatory affairs
Company Website: www.inotiv.com
ASSUMPTION: Inotiv's focus on scientific leadership and ongoing investments enables it to provide a comprehensive range of services and products that exceed client expectations.
📊 Role Analysis
Career Level: This role is at the mid-career level, requiring a Master's degree or higher and at least 2 years of experience in pre-clinical in vivo models of disease.
Reporting Structure: The Scientific Writer II will report directly to the Manager of Scientific Writing and will collaborate with study directors, principal investigators, and other scientific staff across different company sites.
Work Arrangement: This role offers a hybrid work arrangement, with an on-site presence and the option to work remotely for some days.
Growth Opportunities:
- Advancement to a Senior Scientific Writer role with increased responsibilities and leadership opportunities
- Expanding expertise in various therapeutic areas and research models
- Potential to work on diverse projects and collaborate with cross-functional teams
ASSUMPTION: This role provides opportunities for professional growth and development within the company, as well as the chance to work on cutting-edge research projects.
🌍 Location & Work Environment
Office Type: Inotiv's Worthington office is a typical interior office setting, with a hybrid work arrangement available.
Office Location(s): St. Louis MO - Worthington, United States
Geographic Context:
- The St. Louis metropolitan area offers a diverse range of cultural attractions, entertainment options, and outdoor recreation opportunities.
- The region is home to several major corporations and research institutions, providing a vibrant and dynamic business environment.
- The cost of living in St. Louis is generally lower than in other major metropolitan areas, offering affordable housing and a high quality of life.
Work Schedule: Full-time, typically 40 hours per week, with a hybrid schedule option
ASSUMPTION: The hybrid work arrangement allows for flexibility in balancing work and personal responsibilities while maintaining productivity and collaboration with team members.
💼 Interview & Application Insights
Typical Process:
- Online application submission
- Phone or video screening with the HR department
- Technical writing assessment or case study
- In-depth interviews with the hiring manager and team members
- Background check and offer extension
Key Assessment Areas:
- Technical writing skills and attention to detail
- Collaboration and communication abilities
- Understanding of scientific concepts and research models
- Adaptability and problem-solving skills
Application Tips:
- Highlight relevant experience and skills in your resume, focusing on pre-clinical research, data analysis, and technical writing
- Tailor your cover letter to emphasize your fit for the role and Inotiv's mission
- Prepare for the technical writing assessment or case study by reviewing relevant scientific documents and practicing your writing skills
- Research Inotiv's company culture and values to demonstrate your alignment with the organization
ATS Keywords: Scientific Writing, Preclinical Research, Data Analysis, Technical Writing, Attention to Detail, Collaboration, Communication, Inotiv, Drug Discovery, Research Models
ASSUMPTION: Inotiv's hiring process is designed to assess candidates' technical skills, cultural fit, and alignment with the company's mission and values.
🛠️ Tools & Technologies
- Microsoft Office Suite (Word, Excel, PowerPoint)
- Adobe Acrobat
- GraphPad Prism
- Inotiv's proprietary software and templates
ASSUMPTION: Familiarity with these tools and technologies is essential for success in this role, and candidates should be comfortable learning and utilizing new software as needed.
👔 Cultural Fit Considerations
Company Values:
- Play to Win
- Expect More
- Embrace Research and Science
- Impact the Health and Well-being of People All Over the World
Work Style:
- Collaborative and team-oriented
- Attention to detail and commitment to quality
- Adaptable and responsive to changing priorities and deadlines
- Committed to maintaining confidentiality and adhering to company policies
Self-Assessment Questions:
- Do you thrive in a collaborative environment and enjoy working with cross-functional teams?
- Are you detail-oriented and committed to producing high-quality work?
- Can you adapt to changing priorities and meet tight deadlines?
- Are you comfortable maintaining confidential information and adhering to company policies?
ASSUMPTION: Inotiv's company culture values collaboration, attention to detail, and a commitment to excellence in all aspects of the drug discovery and development process.
⚠️ Potential Challenges
- Managing multiple projects and deadlines simultaneously
- Adapting to changes in project scope or priorities
- Working with diverse teams across different company sites
- Maintaining a high level of accuracy and attention to detail in a fast-paced environment
ASSUMPTION: These challenges can be overcome through strong organizational skills, effective communication, and a commitment to continuous learning and improvement.
📈 Similar Roles Comparison
- Unlike other scientific writing roles, this position requires a strong understanding of pre-clinical in vivo models of disease and the ability to analyze and interpret data across various therapeutic areas
- Inotiv's focus on scientific leadership and ongoing investments sets it apart from other research services providers, offering candidates the opportunity to work on cutting-edge research projects
- This role provides a clear career path for growth and development within the company, with the potential to advance to a Senior Scientific Writer position
ASSUMPTION: Candidates should consider their career goals and preferences when comparing this role to similar positions in the industry.
📝 Sample Projects
- Preparing a comprehensive technical report on a pre-clinical pharmacology study, including data analysis, figure creation, and formatting according to Inotiv's style guides and templates
- Collaborating with a study director to develop a protocol for a toxicology study, ensuring all relevant information is included and formatted appropriately
- Reviewing and editing a data package for a regulatory submission, ensuring compliance with applicable FDA guidelines and Inotiv's quality standards
ASSUMPTION: These sample projects illustrate the range of responsibilities and tasks associated with the Scientific Writer II role at Inotiv.
❓ Key Questions to Ask During Interview
- Can you describe the typical workflow for a Scientific Writer II in this role?
- How does this role collaborate with other departments and teams within Inotiv?
- What opportunities are there for professional growth and development within the company?
- How does Inotiv support work-life balance for its employees?
- What is the company's approach to maintaining a diverse and inclusive work environment?
ASSUMPTION: These questions can help candidates better understand the role, the company culture, and the opportunities for growth and development within Inotiv.
📌 Next Steps for Applicants
To apply for this position:
- Submit your application through this link
- Tailor your resume to highlight relevant experience and skills, focusing on pre-clinical research, data analysis, and technical writing
- Write a cover letter that emphasizes your fit for the role and Inotiv's mission
- Prepare for the technical writing assessment or case study by reviewing relevant scientific documents and practicing your writing skills
- Follow up with the hiring manager one week after submitting your application to express your interest in the role and inquire about the status of your application
⚠️ This job description contains AI-assisted information. Details should be verified directly with the employer before making decisions.
