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Katalyst Healthcares & Life Sciences
3.1
Lead Statistical Programmer
Tarrytown, NY
$98K - $143K (Glassdoor est.)
Easy Apply
Develop tools in SAS for data analysis and reporting that comply with regulatory requirements. Create statistical analysis outputs to be used in support of……
8d
statistical analyst jobs in Tarrytown, NY Tarrytown, NY jobs Katalyst Healthcares & Life Sciences jobs in Tarrytown, NY
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Katalyst Healthcares & Life Sciences
3.1
Lead Statistical Programmer
Newark, NJ
Easy Apply
Develop tools in SAS for data analysis and reporting that comply with regulatory requirements. Create statistical analysis outputs to be used in support of……
14d
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ValueBase Consulting
5.0
Senior/Lead SAS Programmer
Minneapolis, MN
$60.00 - $70.00 Per Hour (Employer provided)
Bachelor’s degree in Computer Science, Statistics, Mathematics, or a related field. Familiarity with reporting tools and data visualization platforms.…
30d+
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Gilead Sciences
3.5
Associate Director, Analysis Oversight Lead RWE Safety: Inflammation
United States
$165K - $214K (Employer provided)
This role reports to the CDS-RWE Safety Epidemiologist Lead and partners with CDS-RWE scientific leads and Patient Safety stakeholders to translate safety……
30d+
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Sanofi
4.0
Associate Statistical Project Leader
Cambridge, MA
$122K - $177K (Employer provided)
Best Places to Work
Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to make sure data are……
30d+
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Genentech
4.0
Principal ADS Program Lead
Boston, MA
$136K - $253K (Employer provided)
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As a people leader, the Analytical Data Science Program Lead is accountable for building and developing talent, fostering a culture of technical excellence, and……
30d+
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Genentech
4.0
ADS Lead
Boston, MA
$152K - $283K (Employer provided)
Best Places to Work
You are proficient in programming languages and tools commonly used in clinical data analysis (e.g., SAS, R, Python), with experience implementing scalable,……
30d+
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Katalyst Healthcares & Life Sciences

3.1

Lead Statistical Programmer

Tarrytown, NY

$98K - $143K (Glassdoor est.)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Responsibilities:

Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Assist in establishing standardized programming procedures and work instructions.
Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
Develop and maintain clinical processing workflow systems.
Assist in the development of client proposal documents.
Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.) records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards).
Assist in updating/writing PROMETRIKA standard operating procedures (SOPs).
Develop tools in SAS for data analysis and reporting that comply with regulatory requirements.
Develop specifications (e.g., metadata files), annotate CRFs and create SAS programs for the mapping of raw datasets to CDISC SDTM standards.
Create define.xml files from metadata files for SDTM and ADaM.
Convert data received in other formats to SAS datasets.

Requirements:

Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS.
Knowledge of SDTM, ADaM, FDA and ICH guidance.
Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
Consistent experience as a lead statistical programmer on several concurrent projects.
Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
Excellent analytical skills.
Proven ability to learn new systems and function in an evolving technical environment.
Ability to negotiate and influence to achieve results.
Good presentation skills.
Good business awareness/business development skills (including financial awareness).
Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
Work effectively in a quality-focused environment.
Knowledge of other programming languages and database management software packages is a plus.

See company reviews

Base pay range

The minimum salary is $98K and the max salary is $143K.

$98K – $143K/yr (Glassdoor est.)

$119K

/yr Median

Tarrytown, NY

If an employer includes a salary or salary range on their job, we display it as "Employer Provided". If a job has no salary data, Glassdoor displays a "Glassdoor Estimate" if available. To learn more about "Glassdoor Estimates," see our FAQ page.

Working here doesn’t have to be a secret

3.1

Recommend to a friend
Approve of CEO
CEO: Katalyst HLS
3 Ratings

Katalyst Healthcares & Life Sciences

3.1

Lead Statistical Programmer

Tarrytown, NY

$98K - $143K (Glassdoor est.)

Katalyst Healthcares & Life Sciences

3.1

Lead Statistical Programmer

Tarrytown, NY

$98K - $143K (Glassdoor est.)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Responsibilities:

Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Assist in establishing standardized programming procedures and work instructions.
Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
Develop and maintain clinical processing workflow systems.
Assist in the development of client proposal documents.
Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.) records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards).
Assist in updating/writing PROMETRIKA standard operating procedures (SOPs).
Develop tools in SAS for data analysis and reporting that comply with regulatory requirements.
Develop specifications (e.g., metadata files), annotate CRFs and create SAS programs for the mapping of raw datasets to CDISC SDTM standards.
Create define.xml files from metadata files for SDTM and ADaM.
Convert data received in other formats to SAS datasets.

Requirements:

Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS.
Knowledge of SDTM, ADaM, FDA and ICH guidance.
Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
Consistent experience as a lead statistical programmer on several concurrent projects.
Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
Excellent analytical skills.
Proven ability to learn new systems and function in an evolving technical environment.
Ability to negotiate and influence to achieve results.
Good presentation skills.
Good business awareness/business development skills (including financial awareness).
Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
Work effectively in a quality-focused environment.
Knowledge of other programming languages and database management software packages is a plus.

See company reviews

Base pay range

The minimum salary is $98K and the max salary is $143K.

$98K – $143K/yr (Glassdoor est.)

$119K

/yr Median

Tarrytown, NY

Working here doesn’t have to be a secret

3.1

Recommend to a friend
Approve of CEO
CEO: Katalyst HLS
3 Ratings

Are you open to new opportunities?

10 Lead sas programmer jobs in United States

Base pay range

Working here doesn’t have to be a secret

Base pay range

Working here doesn’t have to be a secret