Associate Director, SAS Macros & Automation (CDISC)
$189k - $220kCSL
CSL is seeking an Associate Director, Programming in King of Prussia, who will lead the design and execution of programming standards. The role involves overseeing SAS macro libraries and ensuring compliance with regulatory standards. Candidates should have over 9 years of experience in clinical programming, strong knowledge of CDISC principles, and advanced SAS macro development skills. This hybrid position requires onsite presence at least three days a week, offering a competitive salary range of $189,000 - $220,000. #J-18808-Ljbffr CSL
$189k - $220k
...difference worldwide. Position Purpose The Associate Director, Programming (Macros & Automation) will design new programming... ...practices aligned with CDISC and regulatory expectations. Responsibilities... ...& Code Ownership – Own existing SAS macro libraries, tools, and...SASWorldwide$189k - $220k
...worldwide. Could you be our next Associate Director, Programming (Macros & Automation)? The job is in our Waltham MA, King... ...practices aligned with CDISC and regulatory expectations across... ...In addition, a deep expertise in SAS macro development to lead and govern...SASWork at officeWorldwide3 days per week$189k - $220k
...worldwide. Could you be our next Associate Director, Programming (Macros & Automation)? The job is in our Waltham MA, King... ...practices aligned with CDISC and regulatory expectations across... ...In addition, a deep expertise in SAS macro development to lead and govern...SASWork at officeWorldwide3 days per week- CSL Plasma Inc. is seeking an Associate Director for Programming, focusing on enhancing... ...programming standards and automation. The successful candidate will oversee SAS macro libraries and engage in cross-... ...to ensure compliance with CDISC standards. With over 9 years of...SASWorldwide
- BioSpace is seeking an Associate Director, Programming in King of Prussia, PA. This hybrid role involves... ...cross-functionally, and developing scalable macro frameworks. The ideal candidate has over 9 years of experience with SAS programming in a CRO or pharmaceutical setting...SAS
- ...Position Summary The Associate Director, Statistical Programming... ...trial data in CDISC format. Coordinating the... ...organization and drive automation of delivery, including... ...pharmaceutical environment using SAS Software.... ...development and use of SAS Macros. Advanced knowledge in...SAS
- ...biotherapeutics leader based in King of Prussia is seeking an Associate Director of Statistical Programming. This role involves... ...or statistical programming, proficient in SAS, and a strong understanding of CDISC standards. Great communication skills and the ability...SAS
- ACL Digital in King of Prussia is seeking a SAS Programmer to develop and enhance SAS codes for CDISC compliant datasets. You will produce statistical analysis outputs for clinical publications and write QC SAS programs following departmental procedures. The role involves...SAS
$181k - $214k
Associate Director, AI & Advanced Analytics CSL’s R&D organization is accelerating innovation to deliver greater impact for patients. With... ...Responsibilities Support development and deployment of AI models, automation scripts, and intelligent agents. Apply agentic software...Worldwide3 days per week- ...emphasizes a project-led structure and collaboration to build a future-ready biotech workforce. Associate Director, AI & Advanced Analytics will lead AI model development, support automation, and partner with R&D teams to prototype high-value use cases; will drive MLOps,...
$170k - $201k
...Data Warehouse, while advancing automation, AI-driven solutions, and... ...standards (e.g., CDASH, SDTM) and associated validation check libraries to... ...through the use of SAS and emerging technologies (e.... ...requirements. Proven expertise in CDISC standards (CDASH, SDTM, ADaM)...SASWork at office3 days per week- ...Allendale Rd., King of Prussia, PA. Responsibilities Write SAS codes to produce CDISC compliant datasets. Create statistical analysis outputs to... ...Reviewers Guides. Develop, enhance, evaluate, and validate standardized macros and utility programs. #J-18808-Ljbffr ACL DigitalSAS
- ...County, North Wales, to support clinical trial data analysis through SAS programming. Ideal candidates will have a Master's degree or... ...collaborating with biostatisticians, and ensuring compliance with CDISC standards. Join us in delivering high-quality analysis for clinical...SAS
$151.5k - $252.5k
As an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and apply QSP models to guide clinical study designs... ...pharmacology tools (such as NONMEM, R, WINNONLIN, Simcyp, SAS). Experience developing mechanistically‑sound PK‑PD models....SASLocal area$150.15k - $250.25k
...Qualifications PhD Experience supporting Oncology Clinical development in pharmaceutical, biotech, or CRO settings Working knowledge of SAS Hands‑on expertise in statistical modeling and innovative methods (e.g., Bayesian approaches) Thorough knowledge of the drug...SASInterim role$118.7k - $209.3k
...domains • Strong and proven understanding of the Engineering development process, specifically agile development, MBE, and Test Automation • Strong process focus with ability to recognize opportunities for improvement and drive required changes Desired skills...Full timeTemporary workPart timeWork experience placementWork at officeRemote workFlexible hours- Merck & Co., Inc. is seeking an Associate Director, Product Manager to own and scale the AI-assisted Content Review capability within the Content & Promotional Lifecycle Automation portfolio. This role drives what gets built, why it matters, and how value is measured across...
- Merck is seeking an Associate Director, Product Manager to scale the MLR review capability within its Content & Promotional Lifecycle Automation portfolio. This role will drive the vision and strategic direction for innovative product development in partnership with various...
- ...quality oversight, and internal readiness. CDISC SDTM/ADaM‑aligned deliverables, including... ...and tooling improvements that enhance automation, data quality, consistency, and efficiency... ...analysis and reporting software (e.g., SAS and/or SQL). Strong understanding of eClinical...SASTemporary work
- ...seeking an IT Senior Auditor to join the SOX Audit Services (SAS) team. SAS serves as Vanguard's centralized ICFR (internal control... ...assessments, system walkthroughs and scoping, testing of IT and automated business process controls, deficiency evaluations, and audit...SASWork at office
- Merck & Co. is seeking an Associate Director, Product Manager to own and scale the MLR review capability within the Content & Promotional Lifecycle Automation portfolio. You will lead AI-enabled review capabilities, align with Brand, Commercial, MLR, Legal, AI, Engineering...
- ...role will lead a global team of digital forensics, incident response and eDiscovery analysts that will: ~ Work closely with the Director, Security Operations to develop and implement a cybersecurity threat analysis structure of common attack techniques to evaluate an...Work experience placementImmediate start
- ...The Associate Director of Business Analytics US I&A is data and analytics leader in support CSL‘s brand teams with strategic insight through quantitative analytics and reporting. The role is to guide the Business Team to proactively plan, design and lead initiatives for...Local area
- ...for clinical trial data analysis. Develop SAS programs to create and validate analysis datasets... ...and validation utilizing global CDISC, ICH, and Therapeutic Areas standards and... ...environment including data step and procedures, macros, graphics, ODS. Interpreting and executing...SASFor contractors
- ...About the Role: As a CBRE Property Management Associate Director, you will be responsible for supervising the team responsible for all operational and financial activities of large portfolios of properties. This job is part of the Property Management job function...Work at officeVisa sponsorshipFlexible hours
$70k - $140k
...Associate Director Of Paid Social Join us as the Associate Director of Paid Social, where you'll be at the helm of crafting and executing dynamic strategies for a major client! Dive into the world of social listening, innovative paid social campaigns, and cutting-edge...Shift work- ...Role Summary The Associate Director, Hematology Commercial Development supports the development and execution of global commercial strategies and tactics for assigned pipeline and early lifecycle assets within the Hematology Therapeutic Area (TA). Reporting to the...Remote work
- ...intelligence to deliver for patients. The Sterility Assurance Associate Director is responsible for leadership, management, and... ...QC microbiology method modernization (eg. rapid methods and automation) in alignment with GSK global strategy Basic Qualifications...Local area
$129k - $203.1k
...(DDT) organization is tasked with the mission to pioneer and deploy innovative digital technologies that drive the acquisition, automation and utilization of data to enhance insights, efficiency, and quality of DSCS processes and methods. Mandate Responsibilities Communications...- ## Associate Director, US Patient AdvocacyBewerbenlocations: Americas, US-Washington DC: Americas, US-PA, King of Prussia, CSL Behringtime type: Vollzeitposted on: Heute ausgeschriebenjob requisition id: R-277529**The Opportunity:**Reporting to the Head of US Patient Advocacy...Work at officeRemote work
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