
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.
🔥 3 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.
• Serve as lead programmer, project lead, or project oversight lead on studies and drug programs • Oversee statistical and bioinformatics programming from clinical trial design through analysis and reporting • Organize teams and implement study strategies for process and programming efficiencies • Create and maintain programs for statistical report generation and validation • Work with project team leaders and client representatives on meetings, timelines, resource forecasting, budgets, and contractual obligations • Plan and contribute to tools and techniques that improve process efficiencies • Represent the department to clients on study matters, bid defenses, and regulatory submissions or reviews • Serve as company project manager on biometrics-only projects when applicable • Provide infrastructure support, conference representation, presentations, training materials, policies, and process improvement • Develop self and junior team members through training, guidance, coaching, and mentoring • Provide employee performance feedback for development, reviews, and training • Encourage industry publications 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 experience, or Bachelor's degree in a related field or equivalent and at least 8 years of experience • An equivalency consisting of appropriate education, training and/or directly related experience may be considered • Strong SAS® programming skills • Understanding of database structures and complex data structures • Excellent written and verbal communication skills, including proficiency in English • Ability to organize and adapt across multiple assignments and changing priorities • Ability to work and lead in a multidisciplinary team setting • Coaching and mentoring capability • Understanding of clinical trials, ICH Statistical and reporting guidelines, and GCP • Knowledge of statistical principles applied to clinical trial design and analysis • Understanding of clinical data submission requirements to regulatory authorities • Project management skills, including project budget creation, updates, and risk management • Ability to interpret and contribute to company policies • Delivery and quality driven
• Collaboration and development opportunities • Global team environment • Scientific excellence-focused work environment
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