Company:
Katalyst Healthcares & Life Sciences
Location: South Plainfield
Closing Date: 17/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities and Requirements:
8 years of experience in clinical trial data analysis using SAS. Preferably in UNIX environment Familiar with Unix command and environment.
Deep knowledge of CDISC Standards and solid ADaM programming experience. Oncology TA experience is preferred.
Ability to quickly learn internal macros, processes and interpret Pinnacle 21 results.
Experienced in supporting ISS, Client ADaM programming and submissions is a plus.
Team player with excellent communication skills and experience working with stat programmers, statisticians and data management personnel.
SAS programming, familiar with SAS language modules e.g. SAS MACRO, BASE, SGPLOT, SQL.
Working knowledge of macro programming; Be able to write macros and able to comprehend existing macros.
Derived Dataset derivation; knowledgeable about the definition or specification files.
High degree of technical competence and communication ability, both oral and written.
Pharmaceutical or related industry experience with clinical trials.
8 years of experience in clinical trial data analysis using SAS. Preferably in UNIX environment Familiar with Unix command and environment.
Deep knowledge of CDISC Standards and solid ADaM programming experience. Oncology TA experience is preferred.
Ability to quickly learn internal macros, processes and interpret Pinnacle 21 results.
Experienced in supporting ISS, Client ADaM programming and submissions is a plus.
Team player with excellent communication skills and experience working with stat programmers, statisticians and data management personnel.
SAS programming, familiar with SAS language modules e.g. SAS MACRO, BASE, SGPLOT, SQL.
Working knowledge of macro programming; Be able to write macros and able to comprehend existing macros.
Derived Dataset derivation; knowledgeable about the definition or specification files.
High degree of technical competence and communication ability, both oral and written.
Pharmaceutical or related industry experience with clinical trials.
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