Biostatistician I
- Mexico
- Biostatistician
- ICON Full Service & Corporate Support
- Hybrid: Office/Remote
About the role
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.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
General Summary for Biostatistician I:
Designs, plans, and executes biostatistical components of clinical studies. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.
Primary Responsibilities:
- Applies knowledge of statistical methodology to ensure proper implementation of clinical studies
- Provides statistical oversight across the whole clinical study. Develops statistical analysis plans and reporting specifications for clinical studies
- Contributes to clinical study protocols and clinical study reports. Reviews reports and underpins the results with statistical expertise
- Accountable for the quality and delivery of the table, figure, and listing (TFL) packages
- Analyzes and interprets results from clinical studies using sound statistical methodology
Biostatistician I Role and Responsibilities:
- Contributes to the development of statistical analysis plans including TFL shells
- Performs statistical analyses under the guidance of other statisticians or independently for simple clinical studies
- Assists with the review of TFLs, tabulation datasets, and derived datasets
- May assist with the development and review of CRFs and edit specifications
- May serve as lead biostatistician for simple clinical studies
- Working knowledge of multiple statistical and therapeutic areas, the drug development process, SAS procedures, and good programming practices
- Ability to plan, implement, and monitor the statistical processes for clinical studies
- Good written and oral communication skills
- Problems are varied and non-routine. Uses previous experience to identify most appropriate solution. Work is performed under general guidance and direction
- Interprets or explains data or information to deliver messages. Requires objective review of difficult work problems, obtaining cooperation or approval
- Contributes to the achievement of goals through personal effort and influence over others. Impact is focused on the achievement of short- to medium-term goals
- Master’s degree in statistics or biostatistics
- 0 years of biostatistical experience
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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 to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect 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 – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil 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, or in order to perform the essential functions of a position, please let us know through the form below.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
Teaser label
Our PeopleContent type
BlogsPublish date
11/05/2014
Summary
Vijayakumar discusses interacting with the SAS community and representing ICON at National and International conferences. I’ve worked for ICON for the last four years and am currently a Senior SAS Pr
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