BioPharma Study Reports Coordinator

Kcasbio; Kansas City (MO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Stock ownership program

KCAS University

Volunteer time off

Job summary

KCAS Bio in Kansas City, MO seeks a Report Coordinator II to compile, format, review, and finalize scientific data and reports from bioanalytical studies. You will work with BioPharma Sciences scientists and study teams, ensuring accuracy, consistency, and compliance with study requirements.

The role involves coordinating report sections, importing data tables, proofreading, meeting deadlines, and maintaining documentation in a fast-paced scientific setting.

Qualifications

• Bachelor’s degree in Biological Sciences, Computer Science, Business Administration, or related field preferred.
• 2–5 years of experience in scientific data presentation or report preparation.
• Proficiency with Word, Excel, and Adobe Acrobat; data management systems experience preferred.
• GLP familiarity and preclinical study protocols preferred.

Responsibilities

• Coordinate preparation, review, and completion of scientific study reports with scientists.
• Compile and finalize report sections, including Materials and Methods and Summaries.
• Import, format, and validate scientific data tables for various study types.
• Proofread reports for technical accuracy and formatting per SOPs and regulations.
• Identify discrepancies and work with staff to resolve issues.
• Monitor deadlines using the Report Tracking Schedule.
• Communicate requirements, timelines, and data needs with study teams.
• Maintain organized report documentation throughout the process.

Skills

Attention to detail

Written and verbal communication

Independent work

Time management

teamwork and collaboration

Education

Bachelor’s degree in Biological Sciences

Equivalent relevant work experience

Tools

Microsoft Word

Microsoft Excel

Adobe Acrobat

Data management systems

Job description

KCAS Bio in Kansas City, MO seeks a Report Coordinator II to compile, format, review, and finalize scientific data and reports from bioanalytical studies. You will work with BioPharma Sciences scientists and study teams, ensuring accuracy, consistency, and compliance with study requirements.

The role involves coordinating report sections, importing data tables, proofreading, meeting deadlines, and maintaining documentation in a fast-paced scientific setting.