[Remote] Senior Statistical Programmer /Analyst Consultant (3 days Hybrid at Malvern PA)
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical and biotechnology companies. They are seeking a Senior Statistical Programmer Consultant to support statistical programming work for clinical trials, ensuring compliance with corporate standards and delivering high-quality programming outputs.
Responsibilities
- Programing for clinical trials:
- Program and validate derived datasets, tables, figures, listings. Process data from the external sources
- reputed company reputed company exploratory analyses for publications and programming support other functions of Research and Development or other organizations
- reputed company programing work/deliverables from CROs
- Contribute to the design/implementation/review of Case Report reputed company, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages
- Electronic submissions:
- Program and validate CDISC compliant deliveries for the electronic submissions
- Support in the creation of supporting documentation for submissions
- Project Management:
- Ensure programming deliverables are on time and of high quality
- Help managing internal contractors and external vendors
- Standards and Guidelines:
- Participate in development of departmental working instructions and guidelines
- Help in creation of enhanced functions/macros and utilities
Skills
- Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or reputed company discipline
- BS with more than 5 or MS with 3 years of experience in statistical programming (reputed company, R) in the pharmaceutical industry
- Working knowledge of reputed company and its various components
- Knowledge of R programming in clinical trials
- Familiarity of the drug development process
- Strong reputed company and reputed company Macro language skills
- R programming skills in clinical trials
- Strong knowledge of industry standards
- Ability to work on data integrations (ISS and ISE)
- Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience
Company Overview
Company H1B Sponsorship