Hiring a Report Writer.
ResponsibilitiesEssential Position Responsibilities:
Ability to navigate critical reporting software systems (MSWord, Excel, Provantis) and work with scanned document image files.Review study protocols and amendments, prepare reporting schedules, and participate in study meetings.Monitor critical phases of study and interact with toxicology staff and subcontractors, as needed, for compliance with protocol, SOPs and applicable regulations. Perform periodic reviews of study data and prepare data summaries for Study Directors and clients as required.Compile data tables and materials/methods for multiple toxicology reports and data packages, concurrently. Verify findings and review raw data, consulting the Study Director regarding any abnormalities.Address applicable findings from QA audits and coordinate receipt of responses from operational groups.Work with Study Director to incorporate client comments into a revised draft.Oversee disposition of study specimens, i.e., test article, formulations, blood samples, preserved tissue.Finalize study report and coordinate archiving activities.Corporate Responsibilities:
Adherence to laboratory health and safetyAdherence to Standard Operating Procedures (SOPs)Adherence to applicable company policies and guidelines Adherence to federal and/or local regulations as applicableAdditional Position Responsibilities: (if applicable)
Assist other Report Writers and Study Directors as needed.Communicate with clients as needed.Perform other duties as assigned.
Professional Responsibilities:(if applicable)
Attend continuing education courses, as appropriate. Qualifications BS/BA degree and/or at least 2 years of experienceExcellent computer, communication and writing skillsAbility to work independently.
Additional Requirements:
Overtime and weekend work as required.Work may require the use of PPE (personal protective equipment)
*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 $60,600- $72,700 and could 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.
Inotiv 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, 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.
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