Senior SAS Programmer job in London, England

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

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Job type: Permanent

Discipline: Statistics

Location: United Kingdom

This vacancy has now expired. Please see similar roles below...

ProClinical is happy to advertise new a UK home-based Senior SAS Programmer role for one of the largest pharmaceutical organisations in the market. This position will focus on developing statistical methods effectively optimising the company.

Job Responsibilities

Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication and/or Health Authorities requests
Be the CDISC SDTM/ADaM expert; use CDISC guidelines to generate SDTM/ADaM datasets
Develop standard SAS macros and prepare the corresponding validation documents
Perform quality check on SAS programs/outputs created by another Statistician/SAS Programmer
Develop SAS programs/macros and utilities for data cleaning
Liaise with Data Management team in identifying and implementing checks according to the Data Validation Plan
Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data
Develop and validate SAS programs for identification of Protocol Deviations
Establish and implement programming rules
Collaborate with Biostatistics and Data Management staff on clinical trials/projects
Prepare, maintain, and archive of SAS programming documentation
Collaborate in establishing and maintaining SOPs related to SAS programming
Collaborate in establishing and maintaining document/programming standards
Contribute to on-boarding of new associates and act as a mentor for junior staff
Keep informed on new SAS developments relevant to the clinical trial data management

Skills and Requirements

Educated to degree level in a relevant discipline and/or equivalent work experience.
Proficiency in SAS.
Extensive knowledge and understanding of the programming and reporting process.
Knowledge of SOP's/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11.
Ability to learn new systems and function in an evolving technical environment.
Strong project management skills.
Ability to successfully lead a global team with proven Lead programming experience.
Competent in written and oral English.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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