
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.
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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.
• Serve as a lead programmer, project lead, or project oversight lead on multiple clinical-trial projects and drug programs. • 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. • Work with project team leaders and client representatives to conduct meetings, maintain timelines, forecast resources, and ensure adherence to budgets and contractual obligations. • Plan and contribute to tools and techniques that improve process efficiencies, including leading solution teams. • Represent the department to clients during study matters, bid defenses, and clinical-data submissions or reviews with regulatory authorities. • Serve as company project manager on projects limited to biometrics services when applicable. • Provide infrastructure support through conferences, department presentations/teaching, training materials, documents, policies, process improvements, and department initiatives. • Increase professional knowledge and skills for self and junior team members in programming, clinical trials, and pharmaceutical-industry developments. • Provide managers with employee-performance feedback for development, reviews, and training. • Increase company visibility through industry-journal articles and conference presentations. • Contribute to department recruitment and candidate interviews.
• MS/MA degree in computer science, statistics, biostatistics, mathematics, or related field and at least 6 years of experience, or bachelor’s degree/equivalent relevant formal academic or vocational qualification and at least 8 years of 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. • Great attention to detail. • Excellent problem-solving and innovative skills. • Excellent written and verbal communication skills, including proficiency in English. • Ability to organize independently and adapt to changing priorities across multiple assignments. • Ability to work and lead in a multidisciplinary team setting. • Positive attitude and ability to work well with others. • 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 management of project budgets and risks. • Ability to interpret and contribute to company policies. • Delivery- and quality-driven approach. • Occasional domestic and international travel may be required.
• Collaboration and development as part of the everyday experience • Reasonable accommodation for individuals with disabilities during the application/interview process and employment • Global team environment • Opportunities to represent the company at industry conferences • Opportunities to present/teach at department meetings • Professional development through training, coaching, and mentoring • Opportunity to contribute to publications and conference presentations
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