Veeva EDC Specialist / Technical Consultant

ActiveSoft, Inc; United States; A distancia; USD 120.000 - 180.000; Jornada completa

Descripción de la vacante

ActiveSoft, Inc is seeking an experienced Veeva EDC Specialist / Technical Consultant to support a clinical systems project for a biotechnology client. The role involves hands-on Veeva EDC configuration, administration, study builds, production support and managing data workflows in a fully remote setting.

The ideal candidate will have strong hands-on Veeva EDC experience, knowledge of study lifecycle activities, validation and CSV/GxP compliance, plus excellent communication with Clinical

Formación

• Hands-on experience with Veeva EDC configuration and administration.
• Experience supporting clinical trials and clinical data management processes.
• Understanding of study lifecycle activities, study builds, and production support.
• Experience troubleshooting EDC configuration issues and system defects.
• Knowledge of GxP/CSV requirements and system validation.
• Strong communication and stakeholder collaboration skills.

Responsabilidades

• Configure and administer Veeva EDC for study builds and data workflows.
• Provide production support and troubleshoot EDC issues.
• Collaborate with Clinical Operations, Clinical Data Management, and IT to deliver solutions.

Conocimientos

Veeva EDC configuration

Veeva EDC administration

Study builds

Production support

Clinical data workflows

GxP/CSV understanding

Strong communication

Herramientas

APIs & integrations

Descripción del empleo

Veeva EDC Specialist / Technical Consultant

Duration: 1 Year Contract with Extension

Remote

Job Overview

We are seeking an experienced Veeva EDC Specialist / Technical Consultant to support a clinical systems project for a leading biotechnology client. The ideal candidate will have strong hands-on experience with Veeva EDC configuration, administration, study builds, production support, and clinical trial data workflows.

This is a fully remote, long-term contract opportunity for someone who can work closely with Clinical Operations, Clinical Data Management, IT, and cross-functional teams.

Required Qualifications

• Strong hands-on experience with Veeva EDC configuration and administration.
• Experience supporting clinical trials and clinical data management processes.
• Understanding of study lifecycle activities, study builds, and production support.
• Experience troubleshooting EDC configuration issues and system defects.
• Knowledge of GxP/CSV requirements and system validation.
• Strong communication and stakeholder collaboration skills.

Preferred Qualifications

• Experience with Veeva Clinical applications, including CTMS and eTMF.
• Experience with APIs and clinical system integrations.
• Veeva certification or equivalent practical experience.