Senior Statistical Programmer
6 days ago Be among the first 25 applicants
Direct message the job poster from Actalent
We are seeking a Senior Statistical Programmer to join a clinical development team. In this role, you will play a pivotal part in the analysis and reporting of clinical trial data, contributing to the success of our research programs. You will collaborate closely with statisticians, data managers, and clinical teams to ensure the accuracy, integrity, and compliance of statistical outputs. This is an excellent opportunity for someone with a strong background in SAS programming and clinical trial analytics to make a meaningful impact in a dynamic and innovative environment.
Responsibilities
* Develop, implement, and maintain programs for the analysis and reporting of clinical trial data.
* Review trial documentation and provide feedback from a statistical programming perspective.
* Define and design project and trial analysis datasets and metadata, including complex derivations and data pooling.
* Collaborate with statisticians and trial programmers to ensure accurate data mapping and analysis.
* Generate Tables, Listings, and Figures (TLFs) in accordance with trial documentation and statistical guidelines.
* Perform and document quality control (QC) checks in line with SOPs and best practices.
* Deliver high-quality outputs to statisticians and clinical teams within project timelines.
* Maintain comprehensive documentation for all programming deliverables and ensure proper filing in the eTMF.
* Provide technical guidance and support to colleagues, and contribute to departmental standards and process improvements.
* Support the implementation of tools and systems that enhance data analysis and workflow efficiency.
* Ensure compliance with ICH-GCP regulations and internal SOPs.
* Lead or contribute to cross-functional initiatives and non-clinical projects.
Must-Haves
* University degree (or equivalent) in mathematics, informatics, or a related scientific field.
* Minimum of 4 years of experience in statistical programming, with at least 3 years in a pharmaceutical or CRO setting.
* Advanced proficiency in SAS programming and statistical analysis for clinical trials.
* Solid understanding of CDISC standards, particularly SDTM and ADaM.
* Basic knowledge of R; familiarity with other programming languages and data management tools is a plus.
* Strong analytical and problem-solving skills with a structured and logical approach.
* Proven ability to work independently and meet deadlines while adhering to SOPs and specifications.
* Excellent communication skills in English, both written and verbal.
* Knowledge of international clinical research regulations (ICH-GCP).
Duration: 12 months
If you want to learn more about this opportunity please feel free to reach out directly to mbertrand@actalentservices.com
*While we appreciate every application, please note that due to the high volume of responses, we may only be able to contact shortlisted candidates.
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Full-time
Job function
* Job function
Information Technology and Science
* Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Actalent by 2x
Get notified about new Statistical Programmer jobs in Allschwil, Basel-Country, Switzerland.
Finance Insights & Data Analyst - PT OBC team member costing expert
Business Analyst / Consultant - Artificial Intelligence & Data - (Data Management & Data Platforms focus) (e/v/e/r/y/o/n/e)
Haut-Rhin, Grand Est, France 2 months ago
Intern Data Science / Management Consulting (m/f/d)
Technical Associate Director Data Architecture
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr