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Intern Manager Statistical Programming Jobs in New York

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

Showing results 41-60

Intern Manager Statistical Programming information

What is the difference between Intern Manager Statistical Programming vs Data Analyst?

AspectIntern Manager Statistical ProgrammingData Analyst
Required CredentialsTypically pursuing or holding a degree in statistics, biostatistics, or related fieldOften holds a degree in statistics, data science, or related discipline
Work EnvironmentPharmaceutical or biotech industry, working on clinical trial dataVarious industries including healthcare, finance, marketing, analyzing data sets
Employer & Industry UsageUsed in clinical research companies, pharma firms, biotech organizationsWidely used across multiple sectors including healthcare, finance, tech

The Intern Manager Statistical Programming role focuses on supervising and managing statistical programming tasks within clinical research, often involving team coordination and project oversight. In contrast, Data Analysts primarily analyze data sets to generate insights across various industries. While both roles require strong statistical skills and familiarity with programming tools, the managerial aspect and industry focus distinguish the Intern Manager Statistical Programming position from a Data Analyst.

What are popular job titles related to Intern Manager Statistical Programming jobs in New York?

For Intern Manager Statistical Programming jobs in New York, the most frequently searched job titles are:

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What cities in New York are hiring for Intern Manager Statistical Programming jobs?

Cities in New York with the most Intern Manager Statistical Programming job openings:

Senior Statistical Analyst

2T Consulting

North Bergen, NJ • On-site

Full-time

Posted 7 days ago


Job description

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians and cross-functional teams to develop ADaM datasets, generate TLFs, support regulatory submissions, and ensure high-quality statistical programming deliverables for clinical studies.

Primary Responsibilities

*Collaborate with statisticians to develop and implement Statistical Programming Plans (SPPs) and Statistical Analysis Plans (SAPs).
*Program, validate, and maintain ADaM datasets, statistical analyses, and programming deliverables using SAS and R.
*Generate and validate Tables, Listings, and Figures (TLFs) for clinical study reports, safety reports, and regulatory submissions.
*Create and maintain programming documentation, including specifications, annotated code, validation plans, and programming guidelines.
*Perform quality control and validation of statistical programming outputs to ensure compliance with CDISC standards and regulatory requirements.
*Support ad hoc statistical analyses, exploratory data analyses, and data visualization requests.
*Develop and maintain reusable programming macros, utilities, and automation tools to improve efficiency and consistency.
*Provide programming support during regulatory submissions, audits, and inspections.
*Collaborate with study teams to resolve programming and data-related issues while ensuring timely project delivery.
*Identify project risks, escalate issues when necessary, and provide regular status updates.
*Mentor and train junior programmers and contribute to continuous process improvement initiatives.
*Stay current with industry best practices, regulatory guidelines, and advancements in statistical programming.

Required Skills & Qualifications

*Strong proficiency in SAS and R programming for clinical trial data analysis.
*Experience programming and validating ADaM datasets, TLFs, and statistical analyses.
*Advanced knowledge of CDISC standards, including ADaM and SDTM.
*Solid understanding of clinical trial processes, statistical methodologies, and regulatory requirements.
*Experience in therapeutic areas such as Oncology, Immunology, Neuroscience, or other clinical domains.
*Strong analytical, troubleshooting, and problem-solving skills.
*Excellent attention to detail with a strong focus on quality and compliance.
*Effective written and verbal communication skills.
*Ability to collaborate with statisticians, clinical study teams, and external stakeholders.
*Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

Preferred Qualifications

*Experience supporting global clinical trials and regulatory submissions.
*Knowledge of clinical data visualization and exploratory data analysis.
*Experience developing standardized SAS macros and programming utilities.
*Prior experience mentoring or leading statistical programming teams.
*Familiarity with FDA, EMA, and ICH regulatory guidelines for clinical data submissions.