Senior Statistical Programmer, Global Regulatory Submissions
Merck
Merck & Co. in Montgomery County, North Wales, is seeking a Senior Statistical Programmer to provide high-quality programming deliverables for global stakeholders. Candidates should have a strong background in SAS and R, with at least 5 years of experience in clinical trials. This role includes preparing compliance programming code for submissions and supporting programming standards development. Benefits include comprehensive health insurance and retirement plans. #J-18808-Ljbffr Merck & Co.
- ...Merck & Co. is seeking an Associate Director in Regulatory Affairs to lead global regulatory strategies for oncology products. The role involves collaborating with global regulatory leads, developing submissions, and engaging with regulatory agencies. The ideal candidate...SeniorRegulatory
- ...ICON is seeking a Senior Manager, Regulatory Strategy to oversee regulatory affairs operations in Whitpain Township... ...clinical trials, managing compliance with global regulatory requirements, and ensuring successful submissions to regulatory agencies. The ideal candidate...SeniorRegulatory
- .... This pivotal role involves coordinating global strategies for Patient-Reported Outcomes and ensuring alignment with regulatory requirements. You will collaborate with cross... ...healthcare outcomes and regulatory submissions, making a real difference in patients' lives...SeniorRegulatory
- ...Malaysia is seeking a programming professional to support statistical programming activities for clinical trial data analysis. The... ...validate analysis datasets for Clinical Study Reports and regulatory submissions. Applicants should have a Master’s degree and relevant...SeniorRegulatory
- Description Lockheed Martin is a global leader in aerospace, defense, and technology solutions, dedicated to pushing the boundaries of... ...tools. Ensure DevSecOps practices comply with legal and regulatory requirements related to information security. Basic Qualifications...SeniorRegulatoryFull time
$117k - $184.2k
...discovery, development, regulatory approval,... ...benefit of patients and global health. Responsibilities... ...high‑quality statistical programming deliverables... ...oncology. The senior statistical programmer gathers and interprets... ...for regulatory submissions, including analysis...SeniorRegulatoryFor contractorsLocal area- Scorpion Therapeutics is seeking a Senior Patent Counsel for their Global Legal Organization. The role is responsible for drafting and prosecuting patent applications, advising on patent and regulatory strategy, and managing IP-related contracts. Qualified candidates should...SeniorRegulatory
- ...patients can resume their lives as quickly as possible. As a Senior Software Engineer, you will be part of a small pluri-... ...documents, and if applicable assist projects lead in the writing of regulatory documents required for product/software certification. · Periodically...SeniorRegulatory
- ...System Validation, focusing on GxP applications. Responsibilities include managing validation activities, ensuring compliance with regulatory requirements, and leading a team to meet quality standards. The position offers the opportunity to work in a dynamic environment...SeniorRegulatory
$61k - $155k
HCLTech is seeking a skilled SAS Programmer in Montgomery County, North Wales, to design efficient data processing utilities and collaborate with biostatisticians. This role requires strong expertise in SAS and a solid understanding of CDISC standards. The ideal candidate...Senior$122k - $198k
...Software Engineer Senior Calling all innovators - find your future at Fiserv. We're Fiserv, a global leader in Fintech and payments, and we move money and information in... ...application status. Fiserv does not accept resume submissions from agencies outside of existing...SeniorWork experience placement- ...subsidiary of Globus Medical) is a global medical device company. We... ...Position Summary : The Senior Firmware Engineer will... ...integrity, patient safety, and regulatory compliance. This role will serve... ...familiarity with FDA submissions preferred. Demonstrated ability...SeniorRegulatory
$1,000 per month
...edge technology and customer-centric solutions. Overview As a Senior Backend Engineer on the Trust Platform team, you'll play a pivotal... ...resilient and reliable systems that meet high security and regulatory standards. Nice to Have Experience working with products related...SeniorRegulatoryTemporary workWork at officeImmediate startRemote workFlexible hours$142.4k - $224.1k
...Description Associate Principal Scientist, Statistical Programming: Provide high quality... ...analysis and reporting deliverables for global PK modeling and simulation... ...graphics for inclusion in study reports and regulatory submissions. Ensure programmatic traceability from...RegulatoryFor contractorsWork at officeLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work3 days per week$40 - $58 per hour
...need for a talented Senior Manager – Real-World Evidence... ...in collaboration with global cross-functional teams, including clinical, regulatory, epidemiology, and... ...Develop protocols, statistical analysis plans, and programming... ...regulatory submissions or health authority interactions...SeniorRegulatoryContract workLocal areaImmediate startRemote work$214.9k - $358.1k
...Role Summary The Global Development Lead (GDL) represents Clinical on the Global... ...to clinical, clinical pharmacology, statistics, safety, commercial, patient access, and... ...of studies in support of worldwide regulatory submissions. The individual will be accountable...SeniorRegulatoryPermanent employmentH1bLocal areaWorldwideVisa sponsorshipWork visaRelocation package2 days per week- Jade Global in Montgomery County, North Wales is seeking a Developer responsible for overseeing web application architecture and migration. The role involves working with Microsoft .NET, Azure, React.js, and more, implementing full SDLC practices. Candidates must possess...Senior
- ...Principal Portfolio Lead, Statistical Programming -... ...mentorship and guidance to programmers and programming team... ...related aspects of regulatory agency inspections and... ...Provides input to submission strategy to regulatory... ...Statistics, Clinical, Global Medical Safety, Project...RegulatoryFull timeTemporary workWork at officeLocal areaRemote work2 days per week
- ...member of myGwork – the largest global platform for the LGBTQ+... ...searching for the best talent for a Senior Principal Scientist,... ...agreements, protocols, reports, regulatory filings as appropriate. Ensure... ...not to affect reporting or submission timelines. Communicate issues...SeniorRegulatoryWork experience placementLocal areaWorldwide
- Scorpion Therapeutics is seeking a Software Engineer with significant experience in Veeva Vault Clinical integrations to design and maintain systems that optimize data workflows and reporting. Your role will involve managing releases, creating API tests, and improving ...Senior
- Roles and Responsibilities Support, maintain, and enhance high-quality software modules within the enterprise product suite. Analyze and resolve software-related issues reported by internal and external stakeholders. Document application specifications...Senior
- ...Senior Manager, Global CapA Management We are searching for the best talent for Senior Manager, Global CAPA Management to join our Quality... ...compliance with all applicable Johnson & Johnson and external GxP regulatory requirements for drug, device and combination products...SeniorRegulatory
- Torrey Holistics is looking for an EDM Programmer-Operator in Hatboro, PA. This full-time role requires expertise in setting up and operating wire and RAM EDM equipment, ensuring high precision in manufacturing. The ideal candidate will have over 5 years of experience,...SeniorFull time
$173.2k - $272.6k
...of diseases. The purpose of Global Labeling is to drive labeling... ...assigned products in line with regulatory requirements and internal... ...to support timely regulatory submissions for assigned products- Leading... ...functional labeling team (including senior management), exhibiting a...RegulatoryFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work- ...recognized for leadership, innovation, and diversity. The future is what you make it. When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers, and doers who make the things that make the future. That means changing the way we fly,...SeniorFlexible hours
$142.4k - $224.1k
...methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. The Clinical Safety Statistics (CSS) group within BARDS supports proactive...RegulatoryFor contractorsWork experience placementLocal areaFlexible hours$137k - $235.75k
...member of myGwork – the largest global platform for the LGBTQ+... ...their merit. Job Function: Regulatory Affairs Group Job Sub... ...Medicine R&D is recruiting for a Senior Manager, North America... ...to and help shape regulatory submission strategies, identifying risks...SeniorRegulatoryTemporary workLocal areaImmediate start$151k - $179k
Job Overview Senior Manager of Technology Transfer... ...Manufacturing, Quality, Regulatory, and Supply Chain... ...inspections, and regulatory submissions Program & Project... ...up and manufacturing Global technology transfer and... ...management, QbD, and statistical tools (DoE) Contract...SeniorRegulatoryContract work- ...studies that are part of a global compound development program... ...GCO, Data Management, Statistics, Regulatory, QMMC, and GMS to ensure flawless... ...of the research, including submission to health authorities. He/... ...develops, in concert with senior clinical staff, credible relationships...SeniorRegulatoryContract workWork experience placement
- ...Genesis AEC is seeking a Senior Mechanical Engineer - Technical Lead - HVAC and Utilities in Whitpain Township, Pennsylvania. This role involves leading HVAC and utility system design, mentoring engineers, and collaborating with project teams in pharmaceutical environments...SeniorFlexible hours
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