Senior Statistical Programmer FSP
Sponsor-dedicated: Working fully embedded reputed company one of our pharmaceutical clients, with the support of reputed company 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 reputed company 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 reputed company your advanced reputed company programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or reputed company 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 reputed company programming
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Production and QC / validation programming
- Generating reputed company reputed company 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 reputed company priorities change
Qualifications
Here at reputed company we want our employees to succeed and we reputed company this reputed company 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 reputed company programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of reputed company experience with a master’s degree or above.
- Study reputed company experience, preferably juggling multiple projects simultaneously preferred.
- Strong reputed company data manipulation, analysis and reporting skills.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Strong QC / validation skills.
- Good reputed company 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 reputed company 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.