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Job Details

Clinical Data Programmer

Company: ICON Plc
Reference: 050186
Closing Date: 20 Aug 18
Type: Full Time
Salary (£): Competitive

Job Summary:

Requirements • EU Proven experience in clinical data programming. • Successfully manage multiple tasks and timelines. • Demonstrated ability to perform assigned tasks individually. • Demonstrated ability to liaise professionally with team members. • Demonstrated ability to learn new technologies, applications and techniques o • Advanced knowledge of the clinical data programming development life cycle, Advanced knowledge of clinical data programming concepts.


Clinical Data Programmer

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As Clinical Data Programmer you are responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables.

• Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets. 
• Create data set specifications per specified study requirements. 
• Program data sets per specification. 
• Validate data sets per the formal, documented CC process. 
• Create data programming specifications per specified study requirements. 
• Program clinical data programs per specification. 
• Validate clinical data programs per the formal, documented CC process. 
• Create and maintain study documentation as required, in accordance with ICON Standard Operating Procedures. 
• Execute programs and generate clinical data outputs to according to study/client requirements. 
• Review and quality assure CRF annotations produced by other programmers. 
• Review and quality assure supporting documentation produced by other programmers. 
• Participate in testing of clinical data system upgrades and documenting of test scripts when required. 
• Adhere to Data Management department quality control procedures. 
• Liaise with other ICON functions & sponsors as needed. 
• To undertake other reasonably related duties as may be assigned from time to time. 
• Contribute to department process improvements, SOPs and WPs 
• Manage programming and validation activities across a single project, ensuring that timelines are met and deliverables are of sufficient quality. 

Apply for this job: Clinical Data Programmer

Contact Information:

Address:  Head Office
South County Business Park Leopardstown, Dublin 18
D18 X5R3
Rep. Ireland
Tel:  +353 1 291 2000
Website:  Visit Our Web Site

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