Clinical Data Programmer II job in

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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. The Clinical Data Programmer is additionally responsible for QC of junior programmer deliverables and assisting with project management activities.

JOB FUNCTIONS/RESPONSIBILITIES:

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 data set and programming specifications produced by other programmers.
Review and quality assure supporting documentation produced by other programmers.

QUALIFICATIONS/EXPERIENCE REQUIRED:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions,

USILATAM/CAN, At least 2 years prior experience in clinical data programming.
EU/APAC: 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.
Team player with strong verbal and written communication skills
Demonstrated ability to learn new technologies, applications and techniques
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 relevant experience required.

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.

Impactful work. Meaningful careers. Quality rewards.

At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential.
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Clinical Data Programmer II

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