Manager, Statistical Programming
Gilead SciencesSalary not specified
Full Time
Expert & Leadership (9+ years)
Not SpecifiedCompensation
Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical, Healthcare, Digital HealthIndustries
Requirements
Candidates must possess a BS/BA in Life Sciences, Computer Science, or a related field, along with a SAS Advanced Certification. A minimum of 10 years of SAS programming experience in the pharma or CRO industry is required, including SAS/Base, SAS/Macro, and SAS/SQL. Additionally, 1+ years of experience in database design and data structures, 5+ years in the pharmaceutical or healthcare industry, and familiarity with CDISC SDTM and Define standards are necessary. Strong organizational, analytical, communication, and time management skills, attention to detail, proficiency in Windows and Microsoft Office, and fluency in English are essential. Experience with other programming languages and working with large, complex patient data sets are considered a plus.
Responsibilities
The Senior Clinical Data Programmer will develop and test SAS code for data file creation, review data specifications, and collaborate with Data Managers to finalize them. Responsibilities include attending client meetings, validating encoding programs, performing ad-hoc programming for quality control and data resolution, and supporting programming for data review. The role involves gaining exposure across modalities, becoming a Subject Matter Expert (SME) in key offerings, and contributing to functional and technical specifications. Additionally, the programmer will participate in audits, represent Clinical Data Programming in NPI processes, identify and implement process improvements, contribute to best practices, act as a CDP SME in cross-functional meetings, mentor new team members, support onboarding, develop SOPs, and complete administrative tasks.
Skills
SAS
SAS/Base
SAS/Macro
SAS/SQL
Database Design
Data Structures
Clinical Data Programming
Data Management
Quality Control
Process Improvement
SOP Development
Clairo
Generates clinical evidence for trials
About Clairo
Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.
London, United KingdomHeadquarters
1972Year Founded
$29.9MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
5,001-10,000Employees