Vacancy expired!
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- Perform analytical programming, data management, quality control and reporting for research projects including clinical trials.
- Extract, manipulate and merge large databases to create analytical datasets.
- Assist in defining analytical variables and help consulting with project staff on project needs.
- Maintain a professional relationship with project personnel.
- Perform simple analytical tasks using SAS or other analytical tools.
- Implement comprehensive quality checking and validation process.
- Maintain and troubleshoot software and programs.
- Design and generate tracking and data entry tools as needed.
- Implement automated reporting and data loading schemes.
- Convert and merge data from a wide variety of sources across platforms.
- Create and maintain documentation to document process and data quality issues.
- Perform other related duties incidental to work described herein.
- One year of related experience with programming and data management using SAS or other computer language.
- Ability to organize and manipulate large datasets.
- Ability to express complex technical information to researchers or to audiences with clinical training.
- Strong analytic and critical thinking skills, writing skills, communication skills, consulting skills, and ability to work within a team. Must be an independent self-starter.
- Both efficient and detail-oriented.
- Master's degree in related field of study.
- Experience with medical or health research.
- Experience with SAS graph, macros, PROC SQL and ODS.
- Knowledge of Unix environment and familiarity of Unix scripts.
- Experience with QA related work.
- ID: #22596892
- State: California Pasadena 91101 Pasadena USA
- City: Pasadena
- Salary: $40 - $50
- Job type: Contract
- Showed: 2021-11-12
- Deadline: 2022-01-09
- Category: Et cetera