Senior Statistical Programmer FSP

hace 3 horas

Bogotá, Colombia Cytel Inc A tiempo completo

## Job Description**Sponsor-dedicated:**Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.**Position Overview:**As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role is fully remote. Experience with oncology is a plus.## Responsibilities**How you will contribute:*** Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming* Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)* Production and QC / validation programming* Generating complex ad-hoc reports utilizing raw data* Applying strong understanding/experience of Efficacy analysis* Creating and reviewing submission documents and eCRTs* Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries* Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.* Being adaptable and flexible when priorities change## Qualifications**Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:*** Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.* At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.* Study lead experience, preferably juggling multiple projects simultaneously preferred.* Strong SAS data manipulation, analysis and reporting skills.* Solid experience implementing the latest CDISC SDTM / ADaM standards.* Strong QC / validation skills.* Good ad-hoc reporting skills.* Proficiency in Efficacy analysis.* Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.* Submissions experience utilizing define.xml and other submission documents.* Experience supporting oncology or immunology studies would be a plus.* Excellent analytical & troubleshooting skills.* Ability to provide quality output and deliverables, in adherence with challenging timelines.* Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. #J-18808-Ljbffr

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