Statistical Programmer Ii
hace 1 mes
Statistical Programmer II, EMEA 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.
At ICON, it's our people that set us apart.
Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership, and Integrity.
We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point.
The role: We are the global biostatistics team dedicated to medical device and late phase research, working on (but not limited to) peri and post-approval research, post-authorization safety studies, observational and non-interventional studies, patient-reported outcomes as well as analyses for abstracts, papers, and manuscripts.
As a Statistical Programmer II, you will be responsible for statistical aspects of clinical and preclinical research projects.
Project responsibilities include study design and case report form review, analysis planning and scheduling, analysis and interpretation of data, and reporting of results.
You may be required to coordinate analysis efforts across multiple research projects conducted for a client.
You will have strong demonstrable experience in: Designing, developing, validating, and documenting SAS programs to generate analysis datasets, summary tables, figures, and listings.
Supporting statisticians in the development and review of Statistical Analysis plans and programming specifications.
Assisting data management with implementing CRFs.
We are looking for: Bachelors or Master's degree in statistics, biostatistics, or related field.
SAS Programming experience – ideally 3 years or more.
Major experience in the Pharmaceutical/CRO industry.
Benefits of Working in ICON: Our success depends on the quality of our people.
That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages, and our annual bonuses reflect the delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans.
Beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfill your sense of purpose and drive lasting change.
ICON 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, please let us know.
What ICON can offer you: In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and 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.
Global Employee Assistance Programme, offering 24-hour access to a global network of professionals.
Life assurance.
Flexible country-specific optional benefits.
Visit our careers site to read more about the benefits ICON offers.
Interested in the role, but unsure if you meet all of the requirements?
We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON.
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