Current jobs related to Clinical SAS Programmer - Carlsbad - Katalyst Healthcares & Life Sciences

  • Clinical Data Analyst

    3 months ago

    Carlsbad, United States Alphatec Spine Full time

    Job DescriptionJob DescriptionATEC Spine is Revolutionizing the Approach to Spine Surgery, a mission that requires continual investigation of clinical requirements and validation of novel solutions. An ATEC Clinical Data Analyst supports the company’s clinical research initiatives by using his/her analytical and statistical skills and experience to draw...

Clinical SAS Programmer

3 months ago

Carlsbad, United States Katalyst Healthcares & Life Sciences Full time
Responsibilities:

Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data.

Generate SDTM domains, ADaM datasets, and Define.xml files .

Assists in creation of table mock–ups under supervision of statisticians.

Reviews output across programs to ensure consistency. Recognizes inconsistencies and initiates resolution of data problems.

Typically creates programs using statistical analysis system language to support the clinical area.

Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures.

Implements data management plans designed to meet project and protocol deadline.

Provides expertise in the design and development of clinical trials, protocols and case report forms.

Acts as a liaison between clinical management, subcommittees and project teams as needed.

Performs other duties as assigned

Requirements:

BS/BA degree in Statistics, Mathematics, or Computer Science or in a related field and 2+ years of Biotechnology/Pharmaceutical/CRO industry experience as a clinical trial SAS Programmer programming CDISC data structures OR.

Master's degree in Statistics, Mathematics, or Computer Science or in a related field and Some experience noted above.

Understands Neurocrine's business objectives and developing understanding of Neurocrine's services and customers.

Has experience in specific functional discipline while working to acquire higher–level knowledge and skills.

Good project management skills.

Knowledge of Biotechnology/Pharmaceutical/CRO industry, specifically clinical trial SAS programming, CDISC data structures.

Strong knowledge of statistical programming tools such as STAT, R, SAS.

Demonstrates knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines.