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Java programmer • springfield il
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Principal Statistical Programmer FSP
CytelSpringfield, IL, United States- Promoted
- New!
ALC Developer Part Time
MAXIMUSSpringfield, IL, United States- Promoted
- New!
Senior Cloud Engineer
TeradataSpringfield, IL, United StatesInformation Systems Advisor I - zOS Systems Programmer Mainframe Network Specialist
Illinois Secretary of StateSpringfield, IL, US- Promoted
- New!
Database Administrator 19-E-02
Illinois Attorney GeneralSpringfield, IL, United StatesRemote Software Engineering Expert - AI Trainer ($50-$150 per hour)
MercorSpringfield, Illinois, US- Promoted
- New!
Staff Android Software Engineer
General MotorsSpringfield, IL, United States- Promoted
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Junior Human Resource Specialist
GAP Solutions, Inc. (GAPSI)Springfield, IL, United States- Promoted
- New!
Tech Lead Engineer, DevOps
iCIMSSpringfield, IL, United StatesRemote Software Engineer III, AI Interview Tools - AI Trainer ($70-$95 per hour)
MercorSpringfield, Illinois, US- Promoted
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Full Stack Java Developer
SynergisticITSpringfield, IL, United StatesSpring Boot/ API Developer - 2 Openings (Hybrid)
DivIHN Integration IncSpringfield, IL, United States- New!
ALC Developer Part Time
MaximusSpringfield, IL, US- Promoted
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Senior Manager - Software Engineering (Health100 Platform)
CVS HealthSpringfield, IL, United States- Promoted
- New!
SharePoint Specialist
ASM Research, An Accenture Federal Services CompanySpringfield, IL, United States- Promoted
- New!
Software Engineer (Technical Leadership)
METASpringfield, IL, United States- Promoted
- New!
Lead Backend Developer for DDoS Protection
OracleSpringfield, IL, United States- Promoted
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Senior Implementation Engineer I
CleoSpringfield, IL, United States- Promoted
- New!
Senior Engineer - AI Platforms
Cardinal HealthSpringfield, IL, United States- live in nanny (from $ 24,375 to $ 390,000 year)
- software architect (from $ 110,000 to $ 245,700 year)
- senior software engineer (from $ 120,442 to $ 234,900 year)
- business operations manager (from $ 89,244 to $ 213,719 year)
- process engineer (from $ 72,500 to $ 207,750 year)
- technical director (from $ 65,750 to $ 205,643 year)
- computer engineer (from $ 66,480 to $ 202,500 year)
- engineering director (from $ 143,810 to $ 202,500 year)
- data architect (from $ 140,400 to $ 201,282 year)
- pediatric dentist (from $ 22,500 to $ 200,000 year)
The average salary range is between $ 87,919 and $ 136,500 year , with the average salary hovering around $ 106,479 year .
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Principal Statistical Programmer FSP
CytelSpringfield, IL, United States- Full-time
Sponsor-dedicated:
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview:
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
As a Principal Statistical Programmer, your responsibilities will include:
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Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
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Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
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Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
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Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
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Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
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Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
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Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
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Participate in the development of CRFs, edit check specifications, and data validation plans
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Provide review and/or author data transfer specifications for external vendor data
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Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
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Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
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At a minimum bachelor's degree in computer science, data science, mathematics, or statistics major preferred
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7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies
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Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment
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Extensive applied experience of CDISC standards (SDTM, ADaM, and Define.xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation
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Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities
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Must be able to work independently
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Outstanding communication skills (written and verbal) and strong leadership skills
Preferred Qualifications (nice to have)
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Prior work experience with pharmacokinetic data and the neuroscience field,
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proficiency in languages or tools other than SAS (e.g., R, Python, and Java, Shiny, Markdown, Unix/Linux and git)
Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.