Veeva CDB Listing Programmer + Jreview

Snaphunt; United Kingdom; On-site; GBP 50,000 - 70,000; Full time

Job summary

A Clinical Research Organisation in the United Kingdom seeks a Clinical Data Programmer to develop data custom listings and support data ingestions into Veeva CDB. The ideal candidate should have 4+ years of experience, excellent SQL skills, and proficiency in several programming languages. The role offers flexible working options and the opportunity to be part of a team with a solid track record in clinical trials.

Benefits

Flexible working options

Growth and learning opportunities

Qualifications

• 4+ years of experience in clinical data programming, particularly with data standards.
• Proficiency in SQL and familiarity with data flow management.
• Hands-on experience in the Clinical Data environment.

Responsibilities

• Develop custom listings based on data cleaning requirements.
• Configure data ingestions into Veeva CDB.
• Collaborate with clinical data providers for testing data transfers.

Skills

SQL programming

Data collection and management

Data quality assurance

Programming in SAS

R programming

JSON

Job description

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Client:

Snaphunt

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

a99c137635d9

Job Views:

6

Posted:

12.08.2025

Expiry Date:

26.09.2025

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Job Description:

The Offer

• Work in a company with a solid track record of performance
• Flexible working options
• A role that offers a breadth of learning opportunities

The Job

Job Description:

Role & Responsibility:

• Develop custom listings based on customer data cleaning requirements using Veeva Clinical Query Language CQL (SQL-based language).
• Configure and support data ingestions (imports) into Veeva CDB
• Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on requirements
• Discuss Veeva CDB best practices with customers' teams, leveraging industry knowledge regarding Clinical Data Programming

The Profile

Required Skills:

• 4+ years of in-depth understanding of data collection, data flow management, data quality, data extraction, and data standards
• Excellent programming skills in SQL is required
• Experience with multiple programming languages (SAS programming language, R, JSON, or other languages/tools) desired, including the creation of EDC database development to new ways of working using technology to accelerate clinical trial setup
• Program listings and mappings
• Create visualizations
• Hands on exposure in reviewing Clinical Data in JReview

The Employer

Incorporated in 1996, Our client is a Clinical Research Organisation supporting trials from Phase II to Phase IV and beyond post-launch of products. Our client offers a range of services, from clinical operations to data services, data analytics and medical writing in compliance with international standards.