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Company | TrialSpark |
Address | New York, NY, United States |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology |
Expires | 2023-09-09 |
Posted at | 8 months ago |
About TrialSpark
- Apply computer science and information technology for the development and maintenance of medium/high complexity tools and related processes supporting the Biometrics analysis and innovation process
- Act as a contributor on cross-functional teams to deliver continuous improvement
- Requires technical skills and adequate industry knowledge to independently perform the programming and project tasks while using judgment about seeking guidance in complex situations
- Support the development and implementation of policies, procedures and objectives for own work or team
- Support evaluations of Biometrics tools and efficiencies in collecting different types of data and production of analyses
- Primarily responsible for providing support to deliver technical programming and information components of moderate scope and medium complexity projects
- Works under the general direction of Biometrics with close collaboration with Clinical Trial/Program Management
- Responsible for supporting medium complex clinical study deliverables or part of project deliverables
- R package development, validation and life cycle management as well as supporting R infrastructure is a plus
- Knowledge and use of data structures such as vectors, matrices, and data frames which help in quick and efficient development
- Educational background in Mathematics, Statistics, Informatics, Life or Social Sciences or equivalent experience in CRO/Pharma
- Excellence in project coordination and managing techniques
- Experience in R and other tools that can ease the process of data reporting & analysis
- The ability to proactively drive innovations
- Understanding of compliance principles preferably supported with an audit experience
- Ability to apply programming expertise to problem solving and quality focused
- Statistical Analysis programming expertise (focus on R, SAS, Python, SQL)
- Experienced in developing efficiencies and improvements in programming utilities and tools
- Enthusiastic, innovative programmer, who can drive cross-functional toolkits for Biometrics deliverables, including dashboards, interactive graphics, and/or FDA deliverables
- Understanding of Clinical Data Management, Statistical Programming, and Biostatistics within clinical trial development & execution
- 2-5 years relevant experience within the Pharmaceutical, CRO or Biotech industry, or equivalent is required, with demonstrated knowledge, experience and ability to perform to meet high quality standards
- Strong working knowledge of SAS programming a plus
- Excellent communication and collaboration skills
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