Associate Clinical Data Science Programmer in Swansea
2 weeks ago
Job ID: JR123164
Associate Clinical Data Science Programmer - Office -based, Swansea or Dublin
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
The Clinical System Developer uses technical, industrial, and interpersonal skills to program the clinical data management system (CDMS) and Non-CDMS components (including dynamic electronic case report form (eCRF) checks, edit checks, custom programs and integrations) and to develop and maintain programs required for handling external vendor data.
As an associate you will be trained, developed and mentored in the following:
Primary Responsibilities:
Reviews the design and assembly of eCRFs.
Reviews and comments on Edit Check Specifications (ECS) and copies and makes modifications to library edit checks when required.
Responsible for the programming of dynamic eCRF functionality and edit checks according to defined specifications.
Responsible for development of custom programs and Data Validation Outputs (DVO) and review of the developed outputs to ensure they meet the agreed specifications.
Reviews Data Transfer Specifications (DTS) and provides constructive feedback. Creates and maintains external data handling instructions and import program specifications. Receives and manages regular imports of data, including blinded and unblinded data.
Contributes to the management of trial deliverables and project scope. Tracks and communicates project development status and worked units to the project team and functional management.
Actively participates in internal meetings and provides constructive feedback to peers, team leads and managers, and functional management.
Responsible for raw data transfers out of the CDMS.
To Be Successful In This Role You Will Have:
Solid knowledge of the requirements, capabilities, and limitations of at least one clinical data management system
Understands pharmaceutical environments and clinical data management system
Good written and oral communication and presentation skills
Benefits Of Working In ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
What ICON Can Offer You:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
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Swansea, United Kingdom ICON Full timeJob ID: JR123163 Associate Clinical Data Science Programmer - Office based, Dublin or Swansea ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future...
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