
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
🔥 0 minutes ago
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10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
• Act as lead programmer, project lead, or project oversight lead on multiple clinical-trial projects • Oversee statistical and bioinformatics programming from study design through analysis and reporting • Organize teams and implement study strategies to improve process and programming efficiencies • Create and maintain programs for statistical report generation and program validation • Represent the department within the company and in interactions with clients and regulatory agencies • Lead studies or drug programs of varying complexity and scale • Conduct team meetings, develop and maintain project timelines, assess and forecast resources, and ensure adherence to study budgets and contractual obligations • Plan and contribute to tools and techniques that improve process efficiencies, including leading solution teams • Represent the department in bid defenses and clinical-data submissions or reviews with regulatory authorities • Serve as company project manager on biometrics-only projects • Provide departmental infrastructure support, including conference representation, presentations, training materials, documents, policies, and initiatives • Develop personal and junior team members’ knowledge of programming, clinical trials, and pharmaceutical-industry developments • Provide employee-performance feedback for development, reviews, and training • Encourage publication of industry articles and conference presentations • Contribute to recruitment and candidate interviews
• MS/MA degree in computer science, statistics, biostatistics, mathematics, or related field and at least 6 years of relevant experience; or bachelor's degree in one of these fields or equivalent relevant formal academic/vocational qualification and at least 8 years of relevant experience • Equivalency through a combination of appropriate education, training, and/or directly related experience may be considered • Strong SAS® programming skills • Strong understanding of database structures and complex data structures • Excellent attention to detail • Excellent problem-solving and innovative skills • Excellent written and verbal communication skills, including proficiency in English • Ability to independently organize, adapt, and adjust to changing priorities across multiple assignments • Ability to work and lead in a multidisciplinary team setting • Ability to coach and mentor others through project leadership • Good understanding of clinical trials, ICH statistical and reporting guidelines, and GCP • Excellent knowledge of statistical principles applied to clinical-trial design and analysis • Good understanding of clinical-data submission requirements for regulatory authorities • Excellent project-management skills, including project-budget creation and modification, and management of project budgets and risks • Ability to interpret and contribute to company policies • Delivery- and quality-driven • Occasional domestic and international travel may be required
• Fully remote work arrangement • Training, guidance, and professional development opportunities • Opportunity to represent the company at industry conferences • Opportunities to present and teach at department meetings • Global team collaboration • Reasonable accommodation for individuals with disabilities during hiring and employment
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