SAS Analyst job at Katalyst Healthcares & Life Sciences Atlanta, GA, US

Job Description

Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

job Description

The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products.
The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity.
The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.

Responsibilities:

Leads the statistical programming activities for projects with lower complexity.
Leads the statistical programming activities for studies.
Develop SAS programs for the creation of ADaM data sets following
CDISC standards.
Develop SAS programs for the creation of Tables, Listings and Figures.
Validation of ADaM data sets, Tables, Listings and Figures.
Create specifications for the structure of ADaM data sets for individual studies and integrated data.
Create documentation for regulatory filings including reviewer's guides and data definition documents
Leads the development of standard SAS Macros and participates in the development of standard operating procedures.
Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.

Requirements:

MS in Statistics, Computer Science or a related field with 6+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience.
In-depth understanding of SAS programming concepts and techniques related to drug development.
Fundamental understanding of CDISC Standards.
Fundamental understanding of the drug development process, including experience with regulatory filings.
Ability to communicate clearly both oral and written.
Ability to accurately estimate effort required for study related programming activities.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Job Tags

Contract work, Immediate start,

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