Data Standard Analyst - Biostatistics Team

Medpace; Cincinnati (OH); On-site; USD 75,820 - 89,200; Full time

Benefits offered by this job

Flexible work environment

Competitive PTO packages, starting at 20+ days

Competitive compensation and benefits package

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Discounts on local sports games, fitness gyms, and attractions

Modern, eco-friendly campus with an on-site fitness center

Discounted tuition for UC online programs

Job summary

A clinical contract research organization in Cincinnati is seeking a full-time Data Standard Analyst to support Biostatistics projects. Responsibilities include implementing SAS programming for data standardization, validation of CDISC SDTM data, and creating annotated CRFs. A Bachelor's Degree in a relevant field is required, and knowledge of SAS programming is preferred. This role offers a competitive salary and a flexible work environment with numerous employee perks.

Qualifications

• Bachelor’s Degree in Math, Statistics, Life Sciences, or any related field required.
• SAS programming knowledge preferred but primary emphasis on analytical skills.

Responsibilities

• Implement edit check specifications via SAS programming to resolve data discrepancies.
• Create annotated CRFs per CDISC SDTM standards.
• Perform validation of CDISC SDTM data according to SOPs.

Skills

SAS programming knowledge

Education

Bachelor's Degree in Math, Statistics, Life Sciences, or equivalent

Job description

Data Standard Analyst – Biostatistics Team

Location: Cincinnati, OH – Salary: $75,820.00–$89,200.00

Join our fast‑growing Medpace team. We’re seeking a full‑time, office‑based Data Standard Analyst to support our Biostatistics projects.

Responsibilities

• Implement edit check specifications via SAS programming to assist with reconciliation of data discrepancies.
• Create annotated CRFs and mapping specifications per CDISC SDTM standards.
• Create SDTM data via SAS programming by implementing data standards for collected study‑level source data.
• Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents.
• Ensure SDTM data conforms to the data standards expected by regulatory agencies.
• Assist with creation of the define package for submission to regulatory agencies.

Qualifications

• Bachelor’s Degree in Math, Statistics, Life Sciences, or equivalent.
• SAS programming knowledge preferred.

Travel

None

Medpace Overview

Medpace is a full‑service clinical contract research organization (CRO) that provides Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach.

Cincinnati Perks

• Cincinnati Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company‑sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Discounts on local sports games, fitness gyms and attractions
• Modern, eco‑friendly campus with an on‑site fitness center
• Structured career paths with opportunities for professional growth
• Discounted tuition for UC online programs

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer
• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Seniority level: Not Applicable

Employment type: Full‑time

Job function: Information Technology

Industries: Pharmaceutical Manufacturing