Essential Responsibilities
- Organizing and providing oversight to internal and external meetings including project meetings, forums/workshops, and conferences
- Develop, write, and edit scientific and technical documents, including workshop reports and scientific manuscripts for publication
- Identification, collection and organization of all available information on alternative toxicological assays including literature and internet searches of public access databases
- Evaluation of statistical data
- Presenting information in public forums
- Providing support to commercial safety assessment projects
Additional Responsibilities
- Technical writing and editing
- Work in a team environment with a professional and positive attitude
- Other duties as needed
Management Responsibilities
Minimum Acceptable Qualifications
Education:
1. B.S. in a related scientific field (preferably toxicology)
2. M.S. in a related scientific field (preferably toxicology)
Experience:
1. 4+ years in scientific writing and editing (preferably toxicology)
2. 1+ years in scientific writing and editing (preferably toxicology)
Skills:
o Excellent organizational skills.
o Strong, proven technical writing and editing skills.
o Ability to exercise independent judgment
o Function well independently or in a team environment.
o Excellent communication skills.
o Computer skills with MS Word/Excel/PowerPoint
o Aptitude or willingness to learn basic coding (such as R or Python) for data organization and pipeline automation
Personnel Supervised
Supervision Received
- Occasional supervision
- Frequent instructions
- Frequent discretionary authority
Working Environment
- Hybrid in office/from home
- Occasional weekend, holiday, and evening work may be required
- Occasional travel required
#LI-JM1
#LI-Hybrid
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 will adjust along with the level of the role to match the person’s relevant experience and/or education level.
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.
