Senior/Principal Statistical Programmer SAS + R (Remote)Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner.

This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials. Xml files for multiple studies ~ Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs ~ Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs ~ Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines ~ Understand and follow FDA regulations which affect the reporting of clinical trial data. Participate in the development of CRFs, edit check specifications, and data validation plans ~ Provide review and/or author data transfer specifications for external vendor data ~ CROs, software vendors, clinical development partners, etc.)



to ensure meeting project timelines and goals ~ Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. At a minimum bachelor's degree in computer science, data science, mathematics, or statistics major preferred ~7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies ~ Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment ~ Xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation ~ Experience supporting regulatory submissions, interacting with the FDA and/or general regulatory authorities ~ Prior work experience with pharmacokinetic data and the neuroscience field, ~ proficiency in languages or tools other than SAS (e.R, Python, and Java, Shiny, Markdown, Unix/Linux and git) Cytel Inc. is an Equal Employment / Affirmative Action Employer.

Senior Sales

Executive, Medical Device Consulting Services, EMEA (Remote) Emergo by UL's Human Factors business unit is a global leader in Human Factors Engineering (HFE) services, with team members in the US, Europe, and Asia. We are seeking a service-minded, customer-centric, proven consultative Senior Sales Executive in Europe to join our team. This senior sales executive will be customer-facing and lead sales of premium HF advisory services in the EMEA region, which requires advanced technical credibility and subject matter expertise to sell and respond to customer inquiries.





This position can be based remotely or in a hybrid model from one of our offices in Barcelona (Spain), Basingstoke (UK), or The Hague (Netherlands). ~ Serves as primary point of contact for specialty Human Factors advisory services throughout sales cycle, from initial contact through project scoping and contract execution ~ Gains Human Factors knowledge quickly via internal training program and independent proactive research, including maintaining knowledge base around Human Factors best practices ~ Bachelor's and/or graduate degree, in business, human factors engineering, biomedical engineering, life science or related field ~ English proficiency must be at least C1 level ~Medical device and/or life science industry experience required ~ Proficient in MS Office (Word, PowerPoint, Excel, Outlook), and CRM software ~ Ability to travel including client visits and working at trade shows, up to 30% A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers' product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers' products and reflects an unwavering commitment to advancing our safety mission.

We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage. Persons are recruited, hired, assigned and promoted without regard to race, color, age, sex or gender, sexual orientation, gender identity, gender expression, transgender status, religion, creed, national origin, ethnicity, citizenship, ancestry, disability, genetic information, military or veteran status, pregnancy, marital or familial status, or any other protected category under applicable law.

📌 Principal Statistical Programmer (Sas + R) - Remote (Real de Gandía)
🏢 Sabores del Mundo Catering
📍 Real de Gandía