The Scientific Writer partners with Study Directors, Principal Investigators, and other scientific staff to write protocols and reports, and generate tables and figures. Maintains templates and style guides and assists in formatting a wide variety of paper, electronic reports, data packages, and other deliverables.
Responsibilities Partner with scientific staff to produce accurate, clear, and concise protocols, reports, and other applicable documentsSetup Provantis, spreadsheets, or other documentation as directed by scientific staff to allow for accurate and efficient data entryCreate “blank” reports with study design and record retention requirements from the study protocol, quote, or other applicable documentationCreate, edit, and format custom tables and figures as directed by scientific staffExport and format tables and figures from applicable software applicationsReview protocols, reports, and other documents for spelling, grammar, clarity, and conformance with applicable style guides and templatesWork with other departments, groups, or teams as necessary to create, format, and issue protocols, reports, amendments, and other required deliverablesConvert deliverables to PDF and format them in compliance with applicable FDA guidelines and Inotiv style guides and templatesCoordinate document signaturesWorking knowledge of study specific services and general facility operations General understanding of relevant regulations (e.g., GLP and GCP)Sense of urgency to ensure that internal and external deadlines are meDetail oriented and capable of producing consistent, error-free, quality deliverablesMaintain thorough knowledge of facility SOPs, policies, study protocols, etc.Excellent communication and interpersonal skills with ability to partner with scientistsPerform other duties as assigned QualificationsSkills and Abilities
Ability to work efficiently with minimal reworkAbility to work independently and as a team memberProficient in applicable computer applications including MS Office and Adobe AcrobatAbility to understand scientific protocols and reportsFollow all SOPs and other applicable laboratory or company policies and proceduresInteract with clients, other employees, and the community in a professional mannerEffective organizational, written, and oral communication skillsAbility to adhere to all company policies, safety regulations and proceduresMaintain confidential informationSupport and participate in other company initiatives as directedAbility to read, write, speak and understand EnglishDemonstrate Inotiv Core Values and adhere to Code of ConductEducation and Experience
Bachelor’s degree or higher (life sciences preferred)Three years or more of technical/scientific writing or other relevant experienceEquivalent combination of related education and required work experience will be considered with Management approvalInotiv has been named a 2023 Top Workplace! 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, sexual orientation, physical or mental disability, genetic information, 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.
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