Report Writer I, Medical Device Pathology

Inotiv•Fort Collins, CO

7d•$56,000 - $65,000•Hybrid

About The Position

At Inotiv, we’re committed to our purpose of helping our clients discover and develop life-changing therapies for people around the world. As part of the medical device pathology team, our Report Writers are crucial to keeping our work efficient and high-quality. We help craft clear, concise reports, make sure our study data is accurate, help push studies to completion, and ultimately improve human health and keep patients safe. To perform this job successfully, an individual must have the knowledge, skills, and abilities identified below and perform each essential duty and responsibility satisfactorily, either with or without reasonable accommodation. The below is intended to describe the general content of and requirements for this job’s performance and is not to be construed as an exhaustive statement of essential functions, responsibilities, or requirements.

Requirements

Bachelor’s degree in science related discipline
Familiarity with writing and interpreting scientific reports and data
Demonstrated proficiency in Microsoft Office Suite (Outlook, Word, Excel) and Adobe Acrobat with ability to quickly learn and master new software applications as needed (Photoshop, InDesign, etc.)
Good organizational skills.
An attitude for quality; detail oriented.
Strong analytical and problem-solving skills; strong mathematical skills is desirable.
Demonstrates an understanding of facility SOPs and Good Laboratory Practice Regulations (21CFR, Part 58) as they relate to study specific services provided, this job description and general facility operations.
A working knowledge and awareness of general laboratory procedures.
Proficient in the use of a computer to compile and maintain simple data, spreadsheets, checklists and reports for records and inventory, utilizing the appropriate software.
Good written and oral communication skills.
Ability to multi-task and prioritize tasks in a high energy, fast paced environment.
Manages time to appropriately meet deadlines.

Nice To Haves

Prior report writing or Quality Control/Quality Assurance experience
One year experience with data analysis in a research setting
One year experience in a regulated environment (FDA and/or GLP)

Responsibilities

Prepares pathology report templates and data spreadsheets to provide a formatted, complete, clear, and concise presentation of results, discussion, and conclusion by the Pathologist.
Performs quality control of study related data entry spreadsheets and reports to ensure accuracy of results.
Ensures scheduled studies are monitored and tracked to meet the objectives, deliverables, and timelines.
Supports local and remote Pathologists, as needed.
Requests and organizes applicable data from the Sponsor/Study Director prior to the Pathologist’s evaluation of slides.
Assists Pathologists in the resolution of audit-related findings.
Provides clear and accurate documentation of study activities according to Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLP) SOP/GLP requirements.
Cross-trains for study work as needed (i.e., necropsy support, histology support).
Performs administrative study tasks (i.e. setting up study binders and slide receipt/inventory).
Follows all standard operating procedures (SOPs) and other applicable laboratory or company policies and procedures.
Maintains confidential information consistent with Inotiv corporate policy.
Supports and participates in company initiatives as directed.
Performs periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs. Participates in SOP writing, reviews, and revisions, as needed.
Completes training requirements as assigned and maintains appropriate training documentation.
Maintains compliance and adheres to all safety regulations, policies, and procedures and good documentation practices.
Interacts with clients, other employees, and the community in a professional manner.
Performs other duties as assigned.