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Senior Clinical Data Programmer

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About the role

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Clinical Data Programmer – Dublin or UK
 
#LI-EZ1
 
 
This is an exciting opportunity to work within a dynamic, 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 work.
Role
  • Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
  • Build data set specifications per specified study requirements.
  • Program data sets per specification.
  • Validate data sets per the formal, documented CC process.
  • Build data programming specifications per specified study requirements.
  • Program clinical data programs per specification.
  • Validate clinical data programs per the formal, documented CC process.
  • Craft 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
  • Lead programming and validation activities across a single project, ensuring that timelines are met and deliverables are of sufficient quality.
Requirements:
  • Proven SQL & SAS programming experience with clinical data management experience.
  • Successfully handle multiple tasks and timelines.
  • Demonstrated ability to perform work you're leading individually.
  • Demonstrated ability to liaise expertly with team members.
  • Team player with strong verbal and written communication skills
  • Proven 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.
  • Associate's degree in information systems, science or related discipline or meaningful experience required
 
*LI-NM1


Benefits of Working in ICON 
Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage. 

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career. 

What’s Next 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity. 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment. 
 
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