Senior SAS Programmer

4 weeks ago

London, United Kingdom MMS Holdings Inc Full time

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma’sinternational awards programs for the last three consecutive years. Senior StatisticalProgrammer
Responsible for implementation and execution of high quality clinical programming
Creates and presents programming training exercises, trains new programmers, and serves as mentor
Interacts directly and independently with client to coordinate all facets of the project; Provides high level of support to the statisticians and medical writers on all programming matters according to client requirements
Generates tables, listings, and graphs from clinical trial databases using SAS
Develops programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software
Develops data and programming specifications jointly with other programmers and biostatisticians
Designs specific data presentations including creative summary tables, graphs, and patient listings
Assists with preparing data validation plan based on customer needs
Reviews data management guidelines for computer edit/validation checks
Independently implements and validates QC findings in compliance with the NC Handling Procedure
Follows processes related to project management as appropriate for programmingprojects (e.g. updating VeoProject, updating PSS, close-out procedures etc)
Demonstrates extensive knowledge of departmental processes (e.g.competency in programming software and willingness to share information)
Leads most projects with minimal management oversight, including complex projects with multiple team members and independent coordination with the client
Demonstrates excellent internal and external leadership skills for projects
Fully accountable for providing highest quality deliverables of entire project to satisfy or exceed client requirements
Ensures compliance to applicable ISMS policies and procedures
Job Requirements (Minimum Education / Experience / Training / Skills)
College graduate in computer science or related field, or related experience
Has high level knowledge of drug development as it pertains to programming; has the ability to apply drug development knowledge during production of high quality programs
Extensive hands-on experience with clinical trials and pharmaceutical development
Strong experience with data and production of TLGs
Extensive experience in pharmaceutical or CRO industry preferred
Thorough knowledge of clinical database structures
Ability to program data presentations, using program such as SAS procedures
Subject matter expert for SAS programming skills; Strong proficiency with MS Office applications

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