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. In short, to be the partner of choice in drug development.
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. 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, generate summary tables, figures and listings.
* Support statisticians in the development and review of Statistical Analysis plans and programming specifications.
* Responsible for 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 yrs or more).
* Major experience in the Pharmaceutical/CRO industry.
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, or in order to perform the essential functions of a position, please let us know through the form below.
#J-18808-Ljbffr