Job Description
The Senior Data Analyst will have responsibility primarily for creating and validating SAS code generated for production of tables, listings, figures, and statistical analyses for internal purposes as deemed necessary by the Company.The Sr. Data Analyst also will be involved in the development and maintenance of integrated clinical databases for biopharmaceutical products under development.
Senior Data Analyst and/or SAS Programmer
Duties and Responsibilities
- Generates analytic code in SAS to execute statistical analyses for study reports, regulatory documents and commercialization and publication activities.
- Validates SAS code produced by other colleagues.
- Develops tables, listings, figures and reports in SAS as needed by the Company.
- Participates in the maintenance and/or development of standard operating procedures and/or business practices related to job activities.
Background Requirements
- Education, Experience, and Knowledge
- A minimum of a Masters Degree in computer science, statistics, operations research or a related field
- Minimum of 5 years experience programming in SAS in a biopharmaceutical environment.
- Experience working with or for Contract Research Organizations in a programming capacity.
- Skills and Abilities
- Excellent verbal and written communication skills
- Ability to work both independently and within teams
- Excellent working knowledge of SAS Stat and Graph
- Some familiarity with other statistical software such as SPLUS
NOTE: This job profile describes the duties and requirements of the position. Requirements stated are representative of minimum levels of knowledge, skills and/or abilities required to successfully perform the job. The employee may be asked to perform other job-related duties as required.
To apply for this position, please visit https://home.eease.com/recruit/?id=469272
Please send resume to jobs@clda.com.
CLINICAL DATA IS AN EQUAL OPPORTUNITY EMPLOYER.
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