176 applicants
K3-Innovations, Inc. · 2 days ago
Lead SAS Programmer
United States
Contract
Remote
Senior Level
8+ years exp
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Hiring Manager
Ilene Brooks
Insider Connection @K3-Innovations, Inc.
Responsibilities
Lead a team of SAS programmers in the development and execution of SAS programs.
Collaborate with project managers and cross-functional teams to define project requirements and timelines.
Provide technical leadership and guidance to team members.
Ensure adherence to project goals, quality standards, and regulatory requirements.
Develop, validate, and maintain SAS programs for data analysis, statistical modeling, and reporting.
Create and optimize data transformation and manipulation routines.
Generate tables, listings, and figures (TLFs) for clinical trial reports and submissions.
Implement advanced statistical techniques when necessary.
Perform quality control checks and validate SAS code to ensure accuracy and reliability of results.
Ensure compliance with industry standards, company SOPs, and regulatory guidelines (e.g., ICH, CDISC).
Create and maintain detailed documentation for SAS programs, data sets, and processes.
Prepare and review documentation for regulatory submissions and audits.
Work closely with data management teams to understand data structures, data validation rules, and data integration requirements.
Collaborate on data cleaning and data transformation activities.
Recruit, train, mentor, and manage a team of SAS programmers.
Conduct performance evaluations and provide ongoing feedback.
Promote professional development and knowledge sharing within the team.
Qualification
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Required
Bachelor's degree in a relevant field (e.g., statistics, computer science, mathematics).
8 – 10 years of experience in SAS programming, including clinical trials or research.
Pharma/biotech/medical device/CRO experience.
Strong expertise in SAS software and programming languages.
Strong knowledge of CDISC standards and experience with SDTM and ADaM datasets.
Proficiency in statistical analysis and modeling.
Excellent communication and leadership skills.
Strong problem-solving abilities and attention to detail.
Preferred
Familiarity with industry regulations (e.g., FDA, EMA) is a plus.
Project management experience is a plus.
Company
K3-Innovations, Inc.
At K3-Innovations, we are passionate about delivering exceptional clinical research services to the bio/pharmaceutical and medical device industries.
51-200 employees
H1B Sponsorship
K3-Innovations, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Trends of Total Sponsorships
2022 (5)
2021 (2)
2020 (2)
Funding
Current Stage
Growth StageCompany data provided by crunchbase
