Prin Statistical Programmer - Real World Evidence

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 Role:Responsible for providing support to ManagerResponsible for leading programmes of work or individual projects of all types.Responsible for performing programming activities according to business SOPs and sponsor requirements.Responsible for all aspects of quality and compliance of assigned projects.Drive efficiency through standards, automation, process improvement and technological advances.Drive efficiency through resource, time line and project management.Responsible for generation of documentation and SAS code required and generation of report tables, listings, figures and datasets.Act as study lead for a project to coordinate all study activities.Ensure projects are conducted in accordance with internal SOPs, client requirements, and Good Clinical Practices (GCP).Review and provide input to project documentation as appropriate including reviewing statistical analysis plans and CRF's.Understand project scope and budget.Carry out quality control checks to ensure compliance with Company and Sponsor requirements.Ensure accuracy of all results and ensure appropriate documentation.Prepare graphs, tables and listings for inclusion in clinical study reports.Write/follow appropriate SOP's and WPS for programming activities.Lead by example to ensure efficient programming practice is maintained.Provide support to the Manager, Statistical Programming.Perform senior review of complete programming deliverables.Ensure compliance with all training requirementsProvide data transfers to company or sponsor standards.Participation in client audits where appropriateAttend and present at external meetings as appropriate.Liaise with Data Management, QA, PK, Medical Writing, Stats and PM.Ensure oversight of packages of work for a sponsor including; lessons learnt between studies, gaining efficiencies through sponsor level automation and standards, leading the technical aspects of sponsor communication/governance, functioning as a single point of contact for project information, addressing any sponsor level quality issues including CAPAs.Provide input to the appraisal process for staff support projects or mentorees.

To be successful in the role, you will have:Doctorate degree or equivalent OR Master's degree and minimum of 4 years of relevant experience OR Bachelor's degree and 6 years of relevant experiencePossess excellent written and oral communication skillsExperienced with macros and arrays for repetitive tasksExperienced with descriptive statistics procedures for summarizing, restructuring, and outputting dataStrong conceptual quantitative and qualitative analytical skillsStrong client management 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 through the form below.

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