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Clinical Research Support Specialist

Veeva Systems
3+ years
Not Disclosed
Remote
1 June 5, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Clinical Research Support Specialist – Veeva Systems

Company: Veeva Systems
Role: Clinical Research Support Specialist
Team: Product Support
Location: United Kingdom (Remote)
Employment Type: Full-Time
Weekend Coverage: Required
Industry: Clinical Research Technology / SaaS / Life Sciences


Role Overview

The Clinical Research Support Specialist serves as a technical and functional support expert for Veeva Clinical products. This role combines clinical research knowledge with product support responsibilities, helping pharmaceutical, biotechnology, and CRO customers resolve issues, optimize system usage, and ensure successful operation of clinical trial technologies.

The position involves direct interaction with customers, troubleshooting complex production issues, collaborating with Development and QA teams, and acting as a bridge between clients and product teams.


Key Responsibilities

Customer & Product Support

  • Provide global support for Veeva Clinical applications.

  • Assist customers with product-related questions and technical issues.

  • Support application navigation, configuration, installation, and functionality inquiries.

  • Ensure timely resolution of customer support requests.

Clinical Technology Support

  • Troubleshoot critical production issues affecting:

    • System availability

    • Data integrity

    • User access

    • Application performance

  • Investigate and resolve complex technical problems.

  • Identify workarounds and long-term solutions.

Issue Investigation & Analysis

  • Gather and analyze information from customers.

  • Replicate issues in test environments.

  • Perform root cause analysis.

  • Document findings and recommended resolutions.

Cross-Functional Collaboration

  • Work closely with:

    • Development Teams

    • Quality Assurance (QA)

    • Product Management

    • Professional Services

    • Sales Engineering

    • Consulting Teams

  • Escalate and coordinate issue resolution when required.

Release & Change Management

  • Support deployment of:

    • New product releases

    • Configuration updates

    • System enhancements

  • Ensure smooth transition of changes into production environments.

Documentation & Knowledge Management

  • Create and maintain support documentation.

  • Update internal tools and knowledge bases.

  • Document troubleshooting procedures and best practices.


Required Qualifications

Education / Experience

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Clinical Research

    • Health Sciences

    • Related disciplines

OR

  • 3+ years of relevant experience with Electronic Data Capture (EDC) systems or clinical research technologies.