Programmer Analyst II

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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, project lead, or project oversight lead on studies and drug programs of varying complexity and scale • Oversee statistical and bioinformatics programming for clinical trials from 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 • 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 contribute to tools, techniques, process efficiencies, solution teams, proposals, bids, and regulatory submissions or reviews • Provide infrastructure support, conference representation, presentations, training materials, department documents, policies, and process improvement initiatives • Increase knowledge and professional skills for self and junior team members • Provide employee performance feedback for development, reviews, and training • Encourage publication of industry articles and conference presentations • Contribute to recruitment and candidate interviews • Provide project leadership and represent the department to clients and regulatory agencies

🎯 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 • An equivalency consisting of appropriate education, training, and/or directly related experience may be considered • Strong SAS® programming skills • Great understanding of database structures and complex data structures • Excellent 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 • Ability to coach and mentor others • Understanding of clinical trials, ICH statistical and reporting guidelines, and GCP • Excellent knowledge of statistical principles applied to clinical-trial design and analysis • Understanding of clinical-data submission requirements for regulatory authorities • Excellent project-management skills, including project-budget creation, updates, budget and risk management • Ability to interpret and contribute to company policies • Delivery and quality driven • Occasional domestic and international travel

🏖️ Benefits

• Collaboration and development as part of the everyday experience • Reasonable accommodation for individuals with disabilities • Equal opportunity employment