Senior Statistical Programmer - Regulatory Data Standards Lead
Merck
Merck & Co. is seeking a Senior Statistical Programmer (SDSQM) to lead submission data standards quality management for worldwide regulatory filings. You will oversee data standards planning, coach project teams, and collaborate with vendors to improve traceability and data fitness. The role emphasizes SDTM/ADaM knowledge, Define.XML, and regulatory submission deliverables, with strong project management and communication requirements across global teams. #J-18808-Ljbffr Merck & Co.
$117k - $184.2k
...provides high quality statistical programming... ...therapeutic areas. The senior statistical programmer will gather and interpret... ..., retrieve required data, transform data into... ...code for regulatory submissions including... ...development of programming standards to enable efficient...SeniorRegulatoryFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- Merck is looking for a statistical programmer to support statistical programming activities for clinical trial data analysis. Responsibilities include developing SAS programs for... ...with biostatisticians and project leads. The ideal candidate should have a Master’...Senior
- Merck is looking for a Senior Scientist, Statistical Programming to support drug and vaccine development projects in North Wales, PA. This role requires strong SAS programming skills and a Bachelor's degree with 5 years of experience or a Master's degree with 3 years. Responsibilities...SeniorRemote jobPart time
- Merck & Co. is seeking a Statistical Programmer in Montgomery County, North Wales, to support clinical trial data analysis through SAS programming. Ideal candidates will have... ..., and ensuring compliance with CDISC standards. Join us in delivering high-quality analysis...Senior
- Responsibilities Support statistical programming activities for clinical trial data analysis. Develop SAS... ...Clinical Study Reports and regulatory submissions (FDA, EMA,... ..., project leads, and other stakeholders... ...and Therapeutic Areas standards and following departmental...SeniorRegulatoryFor contractors
- ...of Prussia is seeking a SAS Programmer to develop and enhance SAS codes... ...datasets. You will produce statistical analysis outputs for clinical... ...working closely with clinical data and generating reports,... ...programming practices meet industry standards. A strong understanding of...Senior
- ...Specialist, Business Analyst, Standards to define AI-consumable standards... .... You will translate complex regulatory needs into structured standards... ...will advise managers and teams, lead governance activities, and collaborate with product, data, and technology colleagues to operationalize...SeniorRegulatory
$117k - $184.2k
Senior Scientist, Statistical Programming Location North Wales... ...trials to worldwide regulatory submissions and... ..., including leading one or more projects... ...CDISC Analysis Data Model (ADaM) and... ...Mentor junior programmers and collaborate... ...CDISC and ADaM standards. Ensuring process...SeniorRegulatoryFull timePart timeFor contractorsLocal areaRemote workWorldwide$117k - $184.2k
...methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical... ...benefit of patients and global human health. The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and...SeniorRegulatoryFor contractorsLocal areaWorldwide- ...Sharp & Dohme is seeking a Sr. Specialist, Business Analyst, Standards to translate regulatory requirements into actionable AI-ready standards and rules... ...-by-design content, and collaborate with product, data, and technology teams. The role emphasizes AI/GenAI enablement...SeniorRegulatory
- ...is seeking a programming professional to support statistical programming activities for clinical trial data analysis. The role requires developing SAS programs... ...analysis datasets for Clinical Study Reports and regulatory submissions. Applicants should have a Master’s degree...SeniorRegulatory
- Merck is seeking a Senior Specialist, Business Analyst, Standards to define and document AI‑consumable standards, rules, and metadata for compliant content creation. You will translate regulatory and policy requirements into clear decision logic and scalable business rules...SeniorRegulatory
- ...seeking a Principal eClinical Data Strategist for its Lansdale location. This senior role focuses on leading the definition and... ...of Clinical Data Management standards and enhancing eClinical solutions... ...including familiarity with regulatory standards. Benefits include...SeniorRegulatory
$65.5k - $134k
...better working world. Senior Analyst - Financial... ...Organization – AI and Data – Service Delivery Center... ..., risk assessment, regulatory compliance) Create RAG... ...visualization, or programming/statistical language Working... ...on high-ethical standards and integrity among its...SeniorRegulatorySummer holidayFlexible hours- ...Write SAS codes to produce CDISC compliant datasets. Create statistical analysis outputs to support final reports, abstracts, posters... ..., and Reviewers Guides. Develop, enhance, evaluate, and validate standardized macros and utility programs. #J-18808-Ljbffr ACL DigitalSenior
- ...business leadership. Ensure adherence to established technology standards, development practices, and SDLC processes. Collaborate with... ...software engineering. Strong experience working with healthcare data. Proficiency in handling and processing large datasets. Strong...Senior
- ...Senior Statistical Manager - (RWE) Peri/Post Approval ICON... ...Manager at ICON, you will lead statistical analysis... ...complex medical data, and contribute to the... ...statistical analysts and programmers to design and conduct... ...methodologies, and regulatory requirements...SeniorRegulatory
- CSL is seeking a Principal, Clinical Data Management Lead to provide leadership and oversight for clinical data build, programming, and... ...outsourced studies. The role ensures alignment with CSL standards, regulatory requirements, and industry best practices. The position...SeniorRegulatory
$105.5k - $175.9k
...services identified through rich data analytics that personalize... ...knowledge of building APIs. The Data Lead will work closely with Patient... .../computer-based work. NON-STANDARD WORK SCHEDULE, TRAVEL OR... ...legal review and statutory or regulatory clarification, which Pfizer intends...SeniorRegulatoryContract workFor contractorsWork at officeRelocation packageWeekend work2 days per week3 days per week- ...tools like Argo CD, Ansible, GitLab CI, and automated security testing tools. Ensure DevSecOps practices comply with legal and regulatory requirements related to information security. Basic Qualifications Final Top Secret Clearance required with the ability to obtain...SeniorRegulatoryFull time
- ...June 30, 2026 at 4:00 AM Senior Software Engineer... ...applications supporting data-intensive workflows. The... ...supports observability standards to improve system transparency... ...issues, recognize statistics staleness, and distinguish... ...critical challenges. Lead technical projects,...SeniorContract workTemporary workWork at office
- ...Experience working with Patient-level and/or medical claims-level data Experience analyzing very large amounts of data Technical... ...and interpersonal skills Qualifications Master's degree/Ph.D. in Statistics, Mathematics or related field with two to five years of experience...Worldwide
- ...design and consulting firm in Plymouth Meeting, PA, is looking for a data analyst skilled in SAS and SQL programming to work with patient data. The ideal candidate will have a Master's or Ph.D. in Statistics or Mathematics, or a Bachelor's with extensive experience in data...
- ...Montgomery County, North Wales. You will define architecture for Salesforce Health Cloud, lead the development of Lightning Web Components, and ensure compliance with security standards. Ideal candidates have deep expertise in Salesforce integrations, HIPAA compliance, and...Senior
- MSD Malaysia is hiring an SAP Master Data Specialist to support Vaccine and Advanced Biotechnologies Process R&D (VAX PR&D) with master... ..., NJ. You will join the PAMS team and help implement data standards, governance, and continuous improvement across sites. #J-18808...Relocation
- ...Martin Rotary and Missions Systems (RMS) as a Senior Software Engineer! Lockheed Martin is a... ..., and a sense of camaraderie. This leads to a positive and productive work culture... ...flexibility to our employees. Schedules range from standard 40 hours over a five day work week while...SeniorFull timeWork at officeRemote workRelocationFlexible hoursShift work3 days per week
- ClinChoice is looking for a Principal Statistical Programmer Consultant in Horsham, Pennsylvania. This role involves developing and maintaining... ...and clinical teams, ensuring deliverables meet standards and participate in study planning. A Bachelor's or Master's...
- ...international defense programs. THE WORK As a Senior Software Engineer, you'll design, develop... ...software products (user authentication, data encryption, application STIGs) and secure... ...to our employees. Schedules range from standard 40 hours over a five day work week while...SeniorFull timeWork experience placementWork at officeRemote workRelocationFlexible hoursShift workNight shiftWeekend work
$126.5k - $199.1k
...portfolio, including interrogation of the data/science through technical reviews and... ...safety, efficacy, quality, and robust supply standards. Develop and maintain strong... ...commercialization, quality, analytical, regulatory, manufacturing, Device Development and Technology...RegulatoryWork at officeLocal areaRemote workMonday to Friday3 days per week$153.8k - $242.2k
...technical team. Responsibilities Lead, mentor, and develop a team... ...portfolio, including data and science reviews and evaluating... ..., quality, and robust supply standards for platforms (e.g., syringes... ..., quality, analytical, regulatory, manufacturing, Device Development...RegulatoryWork at officeLocal areaRemote workMonday to Friday3 days per week
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