CSV Engineer

Intellectt Inc; Redwood City (CA); Hybrid; USD 61,992 - 82,656; Part time

Job summary

A medical technology company is seeking a CSV Engineer for a 12-month contract in Redwood City, CA. The ideal candidate will have substantial experience with Clinical Trial Management Systems (CTMS) and Veeva. Responsibilities include developing UATs, validating Veeva Quality Docs, and reporting findings to upper management. This hybrid role requires a mid-senior level professional with a background in medical equipment and pharmaceutical manufacturing.

Qualifications

• Must have Clinical Trial Management System (CTMS) and Veeva experience.
• Previous experience as a CSV consultant at a pharmaceutical company.
• Prior experience writing test scripts for a CTMS.

Responsibilities

• Provide and develop UATs, periodic reviews, and test scripts for the CTMS Medidata.
• Validate Veeva Quality Docs.
• Report findings to the Associate Director of IT CSV.

Skills

Clinical Trial Management System (CTMS)

Veeva experience

UAT development

Test script writing

Tools

Medidata

SharePoint

Microsoft Office

Job description

Intellectt Inc. provides this range. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base Pay Range

$45.00/hr - $60.00/hr

Direct message the job poster from Intellectt Inc.

Title

CSV Engineer/Clinical Trial Management System (CTMS) and Veeva

Location

Redwood City, CA (hybrid)

Duration

12 month contract

Technology Environment

• CTMS Medidata
• SharePoint
• Microsoft Office – Excel, Word, PowerPoint, Outlook

Responsibilities

• Provide and develop UATs, periodic reviews, and test scripts for the CTMS Medidata.
• Validate Veeva Quality Docs.
• Develop change controls specifically for ServiceNow.
• Report findings to the Associate Director of IT CSV and Associate Director of IT Business Relationships.

Required Skills

• Must have Clinical Trial Management System (CTMS) and Veeva experience.
• Previous experience as a CSV consultant at a pharmaceutical company.
• Prior experience working on CSV for a CTMS.
• Veeva and Medidata (highly preferred).
• Experience validating Veeva Quality Docs.
• Prior experience writing test scripts for a CTMS.

Seniority Level

• Mid‑Senior level

Employment Type

• Contract

Job Function

• Medical Equipment Manufacturing
• Pharmaceutical Manufacturing
• Biotechnology Research