Position: SAS Clinical Programmer

Location: Remote (100%)

Duration: 8+ Months

Position Type: Contract W2

Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc. Healthcare or technology related field.

• 8+ years of SAS programming experience working with clinical trials data in the Pharmaceutical & Biotech industry.

• SAS certifications (Base, Advanced, etc.) are highly desired. Be proficient in Base SAS programming (DATA step), SQL programming (i.e., use of SQL pass-through or PROC SQL), as well as the SAS Macro language for use in making code more efficient.

• Familiarity with programming to generate summary statistics (mean, median, etc.) and complex statistical methods (i.e., SAS GLM, Logistic regression, and survival analysis).

• CDISC data models a necessity, especially SDTM then ADaM

• CDISC knowledge

• SDTM and ADaM dataset experience

• Good written and spoken communications skills in English and thought-leadership skills.

MAJOR RESPONSIBILTIES/ACTIVITIES:

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming. • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).

• Develop SAS programs and generate complete, accurate and validated statistical TLGs in well-defined formats.

• Program SDTM and ADaM datasets according to the dataset specifications.

• Create SDTM annotated patient Case Report Forms.

• Perform data conversion between datasets with two different formats according to conversion requirements/specifications, e.g., converting from Excel data records to SAS datasets, non-CDISC compliant datasets to CDISC compliant datasets.

• Manage electronic data transfers from trial sponsors or other external clinical trial data vendors, such as central laboratories or other specialty laboratories.

• Document data and programming information in accordance with Corporate Governing Documents (Policies, SOPs, or Work Instructions).

• Archive clinical trial data (raw data, SDTM, and ADaM datasets) and programming documentation in accordance with Corporate Governing Documents and/or clinical trial sponsor's specific requirements.

• Write SAS programs to produce tables, listings, and graphs for ad hoc requests, annual progress reports, integrated summaries, publications and other clinical research reports.

• Collaborate with Biostatisticians, Clinical Research Associates, Medical Writers, Regulatory Affairs and Clinical Data Management teams to gather specifications for informative tables, listings and graphs.

• Build SAS data sets from various data sources which meet provided specifications.

• Execute edit/logic checks to assist in data cleaning.

• Maintain and execute programs for the evaluation and validation of incoming clinical data.

• Perform validation of the analysis data sets, tables, listings and graphs.

• Utilize macro libraries and complex data step techniques to standardize programming.

• Maintain and enhance existing programs for clinical studies.

• Gather and analyze programming requirements to develop clinical trial reporting systems.

• Maintain detailed design specifications.

• Ensure that programs and reports follow departmental/company standard operating procedures.

• Assist in the development of departmental systems and generate/maintain systems documentation.

• Participate in the preparation of clinical and statistical summary reports

Job Type: Contract

Pay: $50.00 - $55.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off

Schedule:

• 8 hour shift

Education:

• Bachelor's (Required)

Experience:

• SAS: 8 years (Required)
• SQL: 1 year (Required)
• Leadership: 1 year (Preferred)

Work Location: Remote

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