Hybrid Senior SDTM Programmer/Analyst

at ClinChoice

• Job title: Senior SDTM Programmer/Analyst
• Job type: Full Time
• Experience level: Senior
• Salary: Not specified
• Degree requirement: Bachelor's Degree
• Location requirements: Hybrid, United States

About the role

• Senior SDTM Programmer overseeing SDTM deliverables for regulatory submissions in clinical development. Collaborating with project teams and external stakeholders in a hybrid setting.

Responsibilities

• The Senior Study Data Tabulation Model (SDTM) Statistical Programmer, provides oversight and creation of the SDTM deliverables for analysis and reporting and world-wide regulatory application submissions of drug and vaccine clinical development projects.
• Accountability predominantly includes creation and validation of study data standard deliverables (SDTM dataset, Define.XML, SDRG, aCRF), collaborating with project teams, outreach to external vendors and partners, and keeping current with industry submission data standards.
• The incumbent will be responsible for continuous improvement of our electronic submission process for study data standards deliverables and providing tools and templates to assist delivery focusing on traceability, quality assurance, data conformance and data fitness.
• The position is a key collaborator with statistical programming, statistics, global data management, and other project stakeholders.

Requirements

• BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field with at least 5 years SAS programming experience in a clinical trial environment.
• MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field with at least 3 years SAS programming experience in a clinical trial environment.
• Strong SAS programming skills with demonstrated experience in macro development.
• Demonstrated experience in CDSIC standards with strong command in SDTM.
• Effective interpersonal skills and ability to negotiate and collaborate effectively. Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings). Accountable for tasks at project level; ability to partner with key stakeholders. US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables.
• Knowledge of submission standards CDISC SDTM, Define.XML, SDRG, aCRF.
• Demonstrated success in the assurance of deliverable quality and process compliance. Excels in technical writing, able to convert complex ideas and information into simple readable form.
• Solid project management skills and effective written, oral, and presentation skills.
• Familiarity with data collection and clinical data management concepts and application in SDTM.
• Strategic thinking - ability to turn strategy into tactical activities.
• Ability to anticipate stakeholder requirements

Benefits

• Health insurance
• 401(k) matching
• Flexible work hours
• Paid time off
• Professional development opportunities