Report Writer II at BASI GAITHERSBURG LLC — Rockville, MD

• Purpose of Role / Job Summary: Summary of job: The Report Writer is responsible for preparing accurate, high-quality scientific reports for genetic toxicology studies in compliance with GLP regulations, company protocols and SOPs, and client requirements.

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

Key Accountabilities

Essential Position Responsibilities:

• Responsible for compiling technical/study reports for a variety of assays offered by the Genetic Toxicology department.
• Review lab data workbooks and accurately represent the data in the draft and final reports.
• Responsible for report formatting and submitting reports to QA for auditing.
• Responsible for preparation of appropriate documentation for dispatch of paper copies, if required.
• Responsible for assisting with archiving of raw study data and final reports.
• Accountable for completing and maintaining databases and spreadsheets for reports.
• Must have a broad understanding of writing/editing in Microsoft Word, as well as a working knowledge of assays or tests required to characterize product or material safety.
• Understand scientific observations and ensure that reports meet the generally accepted professional/industry standards.
• Must maintain an understanding of technological principles and applications of the organization’s services.
• Identify and/or resolve issues with study raw data/information appropriately with relevant staff.
• Coordinate and plan work within the report writing team to meet and improve deadlines.
• Obtain required signatures and transfer study reports to the appropriate personnel.
• Communicate daily with other departments to resolve outstanding issues and make sure reports go out on time.
• Assist in the preparation of SOPs and investigation reports relevant to area of report writing responsibility.
• Assist or perform other job duties as assigned.

Professional Responsibilities:(if applicable)

Minimum Requirements:

• Advanced proficiency in Microsoft Word required, including the ability to create, format and edit scientific and technical documents.
• Life Science, Chemicals or Healthcare industry knowledge preferred.
• Knowledge of lab operations, global GLP regulations, and Genetic Toxicology testing guidelines.
• Excellent interpersonal and verbal/written communication skills with the ability to interact with all levels of management and Study Personnel.
• Ability to prioritize, organize and manage time effectively.

Working Conditions & Physical Requirements

• Prolonged periods of working at a computer workstation
• Extended computer and display screen equipment usage
• Ability to read and interpret scientific data and documents
• Ability to communicate effectively in written and verbal formats.

The pay range estimated for this temporary position is $35.00 per hour. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.