Overview
On Site
Full Time
Skills
ISS
Scratch
SAP
Data Collection
Statistics
Computer Science
Mathematics
Clinical Trials
Pharmaceutics
SAS
Data Manipulation
Reporting
CDISC
SDTM
Quality Control
Job Details
Responsibilities:
- Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming.
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs).
- Production and QC / validation programming.
- Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP.
- Demonstrate good understanding of the endpoints and data collection.
- Generating complex ad-hoc reports utilizing raw data.
- Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, or related field.
- 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.
- Proficiency in Efficacy analysis.
- 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.
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