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Intern Principal Statistical Programmer Jobs in New York

Staffingine LLC

Sr. Principal Statistics

Paramus, NJ · On-site

Job Title: Sr. Principal Statistics Job Location: Paramus, NJ Job Type: Contract * The Senior ... Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues ...

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Intern Principal Statistical Programmer information

What does an intern principal statistical programmer do?

An Intern Principal Statistical Programmer assists in developing, validating, and implementing complex statistical programs used in the analysis of clinical trial data. They work under the guidance of senior programmers to perform data manipulation, statistical analysis, and generate summary reports or tables for regulatory submissions. Their role often involves learning industry standards, working with statistical software such as SAS or R, and collaborating with biostatisticians and data managers to ensure data quality and integrity.

What types of projects and responsibilities can an intern principal statistical programmer expect during their internship?

As an Intern Principal Statistical Programmer, you will typically assist with programming tasks related to clinical trial data analysis, such as developing and validating statistical programs using SAS or R. You'll often collaborate closely with statisticians and data managers to ensure data quality and regulatory compliance. Common responsibilities include generating tables, listings, and figures, supporting data cleaning activities, and learning about standard operating procedures. This role also offers exposure to cross-functional teamwork and opportunities to develop technical expertise in a real-world pharmaceutical or CRO environment.

What are the key skills and qualifications needed to thrive as an intern principal statistical programmer, and why are they important?

To thrive as an Intern Principal Statistical Programmer, you need a solid background in statistics, programming (especially in SAS or R), and a relevant degree such as statistics, mathematics, or computer science. Familiarity with clinical trial data standards (like CDISC), data management systems, and regulatory guidelines is typically required. Excellent problem-solving skills, attention to detail, and effective communication are crucial soft skills for success in this role. These competencies ensure accurate data analysis, regulatory compliance, and effective collaboration within multidisciplinary clinical research teams.

What cities in New York are hiring for Intern Principal Statistical Programmer jobs?

Cities in New York with the most Intern Principal Statistical Programmer job openings:

Intern Principal Statistical Programmer jobs near you

Contractor - Principal Statistical Programmer

New York, NY • On-site

Syndax Pharmaceuticals
Biotechnology Research and Development • 51 - 200 employees
Learn more about Syndax Pharmaceuticalsexternal

Full-time

Posted 6 days ago

Job description

Syndax Pharmaceuticals is looking for a Contractor - Principal Statistical Programmer
At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.
The Role:
The Principal Statistical Programmer will provide expert-level hands-on programming support and technical expertise to develop, maintain, validate, and execute SAS programs that access, visualize, analyze, and report clinical trial data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. The Principal Statistical Programmer performs the statistical programming required for analysis of clinical trial data on projects for in-house and out-sourced clinical trials, commercial requests, Health Economics Outcome Research (HEOR) analyses, pooled analysis such as integrated summary of efficacy (ISE) and integrated summary of safety (ISS) and any ad-hoc analyses as required.
The candidate will have a proven ability to work independently, possess excellent communication skills, and have advanced expertise in SAS programming.
Key Responsibilities:
  • Supports study leads and take ownership of multiple deliverables within a drug program whilst providing support across various drug platforms.
  • Acts as an integral member of project team, complementing the lead programmer as required. May attend project team meetings as required and will cross-collaborate with vendors, biostatisticians, data managers, and other cross-functional teams as required.
  • Serve in a primary role for production of all tables, listings, and figures, and Case Report Form (CRF) tabulations for clinical trial programs including ISS/ISE.
  • Serve as a primary programmer to support regulatory requests, commercial requests, ad hoc analyses, biomarker analyses, HEOR analyses etc.
  • May review critical Standards Artifacts and Processes (such as Statistical Analysis Plans, Data Validation Plans, eCRFs, etc.) and provide constructive comments.
  • Troubleshoots and provides quality review of complex SAS programs.
  • Follows good programming practices and adequately documents programs.
  • Understands and follows FDA regulations which affect the reporting of clinical trial data.
  • May participate in cross functional task forces and initiatives representing Statistical Programming.

Desired Experience/Education and Personal Attributes:
  • At least eight years of relevant experience. Exceptional candidates with 5+ years of experience may be considered.
  • Bachelor's degree.
  • Experience in Oncology required; Leukemia experience preferred.
  • Ability to communicate technical concepts clearly and concisely to non-technical colleagues.
  • Successfully completed several large or complex projects.
  • Ability to handle multiple projects with aggressive timelines.
  • Ability to multitask and prioritize work.
  • Excellent knowledge of SAS.
  • Familiarity with coding dictionaries (WHO, MedDRA).
  • Expert at industry standard initiatives such as CDISC.
  • Knowledge of medical and statistical terminology.
  • Capable of using Windows, Word, and Excel.

Location: While our corporate headquarters are located in New York City, this position is open to candidates from any location with a preference for east coast locations.
About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company's pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
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