Advanced Clinical is a global clinical development organization that provides CRO, FSP, Quality & Validation, and Strategic Resourcing services for biopharmaceutical and medical device organizations. Our mission is to deliver a better clinical experience for our clients. With global experience in over 50 countries, we are committed to improving all lives touched by clinical research. We understand the complex nature of the clinical research industry and approach each opportunity with compassion. Together, we answer the hopes of patients and healthcare professionals with industry-leading services in global life-sciences. As part of the Advanced Group family of companies, Advanced Clinical employees provide the support, structure, and professional background and experience for better clinical trials and research. They are the foundation of our energetic and collaborative environment, where constant learning and service to others take top priority. We seek dynamic, hard-working team members who are inspired to work amongst diverse backgrounds and perspectives. From our altruistic mission to outstanding career development opportunities, there's no better place to grow your career than Advanced Clinical.
NOTE: This role can be based remotely from any U.S. location.
The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming support for clinical trials and contributing to the development of departmental standards. This includes developing and validating SAS programs for statistical tables, data listings, figures, and derived datasets according to specifications.
- Follow Standard Operating Procedures (SOPs)
- Understand and implement CDISC and other regulatory standards.
- Develop and implement internal SAS programming standards.
- Create and maintain specifications for CDISC SDTM and ADaM datasets and other derived datasets.
- Apply knowledge of SAS programming to develop and validate statistical tables, data listings, figures, and derived datasets (including STDM and ADaM datasets) for clinical trials data and for integrated summaries according to SAP and other specifications.
- Review annotated case report forms and database structures.
- Perform ad hoc analyses of current and legacy databases.
- Work closely with other programmers, statisticians, data managers, and database programmers to ensure accurate and high-quality deliverables.
- Support the efforts of others and share knowledge and skills.
The ideal candidate should have a degree in Statistics, Computer Science or a closely related field, with a minimum of 3 years of experience as a SAS programmer, and a minimum of 2 years of experience in a CRO or pharmaceutical company. The candidate should have knowledge of basic statistical concepts, must have strong SAS programming skills, including data manipulation and statistical analysis procedures, and must have experience with Word, Excel, and PowerPoint. Experience in mapping SDTM datasets is a strong plus. Excellent communication skills (both oral and written) and organizational skills are required. Candidate must be detail-oriented, team-oriented, and self-motivated, and must work well under pressure. What's in it for you?
Advanced Group offers competitive compensation, comprehensive benefits packages, and a flexible work environment designed to help our team members and their families stay healthy, meet their financial goals, and generally thrive in and beyond work. Visit the links below to discover all that Advanced Group has to offer: Our Culture:
https://careers.advancedgroup.com/embrace-our-culture Career Development Opportunities:
https://careers.advancedgroup.com/realize-your-potential Community Programs:
For a complete list of all of our job openings, please visit Advanced Group's career site here .
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