Senior Statistical Programmer 1 - Europe - Remote
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Who We Are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, a global team of over 3,500+ experts dedicated to changing the way the world experiences CROs. Our mission is to work with passion and purpose every day to improve lives, and we value diversity and inclusion in a collaborative environment.
What The Statistical Programming Department Does At Worldwide
As a member of our Biostatistics and Statistical Programming team, your programming, analytical skills, and ability to process and interpret data are essential. You’ll grow your knowledge of SAS and CDISC standards across all phases of clinical trials, work directly with sponsors, data managers, statisticians, programmers and the study team across therapeutic areas including cardiovascular, metabolic, neuroscience, oncology and rare diseases. You will have hands-on involvement with the autonomy to do your work, with support to succeed and grow, and the work will matter.
What You Will Do
* Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures and listings (TFL).
* Review and provide guidance on the development of the clinical database specification, data transfer agreement/specification, and specification of tables, figures and listings (TFL) shells.
* Develop and review specifications for SDTM and ADaM datasets for safety data, TFL shells and other specifications (e.g., patient profiles, OPS reports).
* Develop and review electronic submission packages (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer's Guide) for high-complexity studies.
* Serve as a programming project lead on complex studies (e.g., adaptive design, integrated safety/efficacy) to distribute and oversee tasks, communicate with clients, plan and execute delivery, and manage resources and project priorities while ensuring budget and scope alignment.
* Provide consultancy to Clinical Data Managers, Statistical Programmers and Biostatisticians on programming, clinical and analysis data standards (CDISC) and electronic data submission requirements.
Your Experience
* Educated to degree level or equivalent.
* Advanced SAS programming skills with expert knowledge in SAS/Macro, Proc Report and ODS; good working knowledge in SAS/Graph, Proc SQL, SAS/STAT.
* Minimum 4 years of related experience.
Your Capabilities
* Computer literate and numerate with the ability to adapt to various computer systems.
* Hands-on expert-level project statistical programmer with experience providing programming leadership.
* Strong analytical skills, attention to detail, and ability to deliver with customer focus and collaboration.
Employment Details
* Employment type: Full-time
* Seniority level: Mid-Senior level
* Job function: Research, Analyst, and Information Technology
* Industry: Research Services
Worldwide is an equal opportunity employer committed to diversity and inclusion. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other protected class.
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