ClinChoice - Senior Statistical Programmer - should be proficient in R (Permanent role )
Requirements
• Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline. • BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry. • Working knowledge of SAS and its various components. • Knowledge of R programming in clinical trials • Familiarity of the drug development process. • Strong SAS and SAS Macro language skills. • R programming skils 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. • The Application Process • Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. • Who will you be working for? • ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. • Our Company Ethos • Our Company Ethos • Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
Responsibilities
• Programing for clinical trials:Program and validate derived datasets, tables, figures, listings. Process data from the external sources. Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations. Oversee programing work/deliverables from CROs.Contribute to the design/implementation/review of Case Report Form, 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. • Programing for clinical trials: • Electronic submissions: • Project Management: • Standards and Guidelines:
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