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Scientific Report Writer

Envigo, an Inotiv Company

Scientific Report Writer

Gaithersburg, MD
Full Time
Paid
  • Responsibilities

    Job Description

    COMPANY OVERVIEW

    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.

     

    CORPORATE RESPONSIBILITIES

    • Adherence to laboratory health and safety
    • Adherence to Standard Operating Procedures (SOPs)
    • Adherence to applicable company policies and guidelines
    • Adherence to federal and/or local regulations as applicable

    ESSENTIAL POSITION RESPONSIBILITIES:

    • Ability to navigate critical reporting software systems (MS Word, 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 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.

    OTHER RESPONSIBILITIES

    • Assist other Report Writers & Study Directors as needed
    • Communicate with clients as needed.
    • Perform other duties as assigned.

    PROFESSIONAL RESPONSIBILITIES

    • Attend continuing education courses, as appropriate.

    QUALIFICATIONS

    • BS/BA degree, or at least 2 years of experience
    • Excellent computer, communication and writing skills
    • Ability to work independently
    • Willing to work weekends and OT as needed

     

    Company Description

    Where insights lead to answers. Inotiv careers are dynamic, meaningful and have an extraordinary impact on people's lives. Join our team and help drive innovations forward. analyze. answer. advance. Inotiv is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.