# Senior Clinical Systems Designer (Veeva Library)

**Company**: ICON Strategic Solutions
**Location**: Chennai
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Chennai/Sr-Clinical-Systems-Designer--Veeva-Library-_JR163552?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/senior-clinical-systems-designer-veeva-library-79aa49cf-f62/

## Description

As a Senior Clinical System Designer at ICON, you will design and implement advanced clinical systems that enhance trial design and execution.

Key Responsibilities:

- Design, develop, validate, and maintain reusable eCRFs and library components within Veeva EDC.

- Create and maintain eCRF specifications, edit-check specifications, dynamics, and derivations.

- Establish library collections, version control, change management, and governance processes.

- Ensure library components align with clinical data standards and protocol requirements.

- Optimize library design to balance reusability, study needs, and ongoing maintenance.

- Support lab modules and integrations with IRT, safety, coding, local laboratories, and other clinical systems.

- Develop and execute UAT scripts and validate EDC configurations.

- Understand how library components are consumed and implemented at the study level.

- Troubleshoot database and library-configuration issues and implement post-production changes.

- Understand backend EDC data, raw/CDM outputs, SDTM structures, and downstream data-model requirements.

- Partner with Data Management, Standards, Clinical Operations, Clinical Supplies, IT, Quality, CROs, and technology vendors.

- Support EDC standards, governance models, inspection readiness, and TMF documentation.

- Identify opportunities to automate and streamline the specification-to-build process.

- Track deliverables, milestones, risks, and quality metrics.

Required Skills and Experience:

- Bachelor’s degree or equivalent relevant experience.

- 6+ years of experience in Data Management, EDC programming, Clinical IT, or related clinical-research functions.

- 3–5 years of hands-on Veeva Library development and maintenance experience.

- Strong hands-on experience with Veeva EDC is mandatory.

- Experience in eCRF design, EDC programming, edit checks, dynamics, derivations, and lab modules.

- Knowledge of clinical data standards and protocol interpretation.

- Experience with reusable components, library collections, version control, and governance.

- Understanding of blinded and unblinded study configurations.

- Experience integrating EDC with laboratories, safety systems, IRT, coding, and other clinical-trial modules.

- Understanding of raw/CDASH, SDTM structures, and downstream data consumption.

- Experience with CQL, CDB, JSON, or C# is preferred but not mandatory.

- Understanding of CTMS, SAS, R, Python, data warehouses, or SharePoint is advantageous.

Other Requirements:

- Independent lead contributor who can translate broad requirements into workable solutions.

- Ability to think beyond provided specifications, challenge assumptions, and recommend improvements.

- Strong problem-solving, stakeholder-management, and cross-functional collaboration skills.

- Ability to deliver confidently with limited supervision and reduced review cycles.

Rewards & Benefits:

- Competitive base salary and performance-related incentives

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable

- Retirement and pension plans

- Life assurance and disability coverage

- Employee assistance programmes and wellbeing resources

- Learning and development opportunities through structured training and career pathways

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## Skills

### Required
- Veeva EDC
- eCRF design
- EDC programming
- clinical data standards
- protocol interpretation
- CQL
- CDB
- JSON
- C#
- CTMS
- SAS
- R
- Python

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