Programmer Analyst II

🔥 12 minutes ago

🇨🇳 China – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Serve as lead programmer or project lead on studies or drug programs of varying complexity and scale • Oversee statistical and bioinformatics programming aspects of clinical trials from design through analysis and reporting • Conduct team meetings with project leaders and client representatives • Develop and maintain project timelines, assess and forecast resources, and ensure adherence to study budgets and contractual obligations • Plan and provide developments to tools and techniques that improve process efficiencies • Lead solution teams and contribute to process and tool improvement efforts • Represent the department to clients on study matters, bid defenses, and clinical-data submissions or reviews with regulatory authorities • Contribute directly to proposals and bids • Serve as company project manager on biometrics-only projects when applicable • Provide infrastructure support, conference representation, department presentations and teaching, training materials, documents, policies, and department initiatives • Increase professional knowledge and skills for self and junior team members • Provide feedback to managers on employee performance, development, reviews, and training • Encourage publication of articles and conference presentations to increase company visibility • Contribute to recruitment and candidate interviews

🎯 Requirements

• 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 • 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 • Attention to detail • Problem-solving and innovative skills • Excellent written and verbal communication skills • Proficiency in the English language • Ability to organize, adapt, and adjust to changing priorities across multiple assignments • Ability to work and lead in a multidisciplinary team setting • 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 for regulatory authorities • Project management skills, including project budget creation, updates, and management of project budgets and risks • Ability to interpret and contribute to company policies • Delivery and quality driven

🏖️ Benefits

• Collaboration and development opportunities • Global team environment • Passion, innovation, and commitment to scientific excellence