Programmer Analyst II
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Job Description
Programmer Analyst leading SAS and statistical programming for Thermo Fisher Scientific’s clinical trials. Overseeing projects, regulatory submissions, budgets, and junior-team development.
Responsibilities:
- 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
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