Job
- Level
- Senior
- Job Field
- Data
- Employment Type
- Full Time
- Contract Type
- Permanent employment
- Location
- Oberwöhr
- Working Model
- Hybrid, Onsite
Job Technologies
Your role in the team
- Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), 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 using raw data
- Applying strong understanding/experience of effectiveness 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
- Performing lead when called upon
- 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
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Our expectations of you
Education
- 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.
Qualifications
- Strong SAS data manipulation, analysis and reporting skills.
- Strong QC/validation skills.
- Good ad hoc reporting skills.
- Proficiency in effectiveness analysis.
- 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.
Experience
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- 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 Rare Diseases and Gastro Intestinal studies would be a plus.
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Job Locations
Location Oberwöhr
Bayern
Germany
This is your employer
Cytel
We provide unrivaled biostatistics and operations research knowledge to our customers. Our knowledge is available in the form of both software and services. This knowledge, supported by our trial implementation capabilities, is what makes us different. We are leaders in the design and implementation of adaptive clinical trials.
Description
- Founding year
- 1987
- Company Type
- Established Company
- Working Model
- Hybrid, Onsite
- Industry
- Pharmaceutical Sector, Chemical Industry, Biotech
Senior Developer Data
- Location
- Oberwöhr
- Working Model
- Hybrid, Onsite
