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Clinical Data Programmer

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About the role

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Clinical Data Programmer I
 
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.  Our Clinical Data Programmer will be responsible for Electronic Case Report Form (eCRF) related aspects of Database Administration.  Responsibilities extend to SAS programming of deliveries and edit checks.
 
Overview of the Role
  • Collaborates with Project Team to agree on vendor expectations for the collection and transfer of data.
  • Responsible for configuring the data loading tools based on data collection specifications.
  • Represents Data Management at UAT handover meetings.
  • Performs creation of outbound data deliveries, verification of file format, and reports errors to Project Data Lead.
  • Performs verification of inbound data file formats and content and loading of data for the blinded presentation to the reviewer
  • Installation of eCRF databases and preparation of databases for review sessions
  • Database maintenance.
  • Execute database change requests.
  • Maintenance of randomization schemes for blinded presentation of data to reviewers.
  • Prepare database queries for ad- hoc reports
  • Creation of delivery programs
  • Creation, testing, verification and implementation of edit check programs
  • Code review of colleagues work to ensure consistency and viability of logic
  • Provide technical assistance for documentation efforts
  • Travel (approximately 5%) domestic and/or international
 
Role Requirements / Skills / Experience Required
  • 1 – 2 years SQL programming experience
  • SAS experience preferred
  • Proficiency in Microsoft SQL Server
  • Trained in computerized systems in Clinical Trials
  • Proficiency in Business computer skills
  • Documentation skills
  • Thorough knowledge of ICH Guidelines and GCP including regional regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing
  • Excellent oral and written communication and presentation skills.
  • In depth knowledge of clinical trial process and data management, clinical operations, and systems applications to support operations.
  • Demonstrated organizational skills to handle multiple competing priorities simultaneously across an assortment of projects and initiatives.
 
Benefits
 
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  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 if you are successful you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of 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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