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Sr Statistical Programmer

Initial Therapeutics, Inc.

Basking Ridge (NJ)

On-site

USD 92,000 - 152,000

Full time

11 days ago

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Job summary

An established industry player is seeking a skilled programmer with a strong background in statistics and data analysis. In this role, you will support and lead programming efforts for clinical trial data, ensuring compliance with industry standards. You'll work within a multidisciplinary team, contributing to the development of tools and process improvements while providing timely support for analysis and reporting. This inclusive company offers a diverse culture and comprehensive benefits, making it an exciting opportunity for those looking to make a meaningful impact in the biotechnology sector.

Benefits

Health and wellness programs
Fitness centers
Equity awards
Annual bonuses
Paid time off

Qualifications

  • Masters Degree or MS in relevant fields with 3+ years of programming experience.
  • SAS Certification is desirable.

Responsibilities

  • Support and lead programming and QC of analysis datasets and TFLs.
  • Integrate data across studies and manage programming specifications.

Skills

Programming
Data Analysis
Statistical Analysis
SAS

Education

Masters Degree in Statistics
MS in Computer Science
MS in Mathematics
MS in Engineering
MS in Life Science

Tools

Regeneron tools

Job description

JOB RESPONSIBILITIES:

  1. Support and/or lead programming and QC of analysis datasets, TFLs, or standard tools following Regeneron standard data models or user requirements. Assist in coordinating activities and communicating shifting timelines and milestones.
  2. Integrate data across studies to support CSS/CSE. Create, manage, and maintain programming specifications for analysis datasets utilizing Regeneron tools and methodologies.
  3. Support the creation and validation of submission requirements (e.g., annotated CRF, data export files, define documents).
  4. Work within a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch, and annual reports. Develop and provide department training for applications and tools if applicable.
  5. Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist with more complex data presentations.
  6. Participate in department working groups; contribute to the development of tools and process improvements.

JOB REQUIREMENTS:

Education

Masters Degree or MS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline with 3+ years of programming experience, preferably in processing clinical trial data within the biotechnology, pharmaceutical, or health-related industry.

SAS Certification is desirable.

Experience

3-5 years of relevant experience.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We offer an inclusive and diverse culture with comprehensive benefits, which may include health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels.

Regeneron is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, nationality, ethnicity, civil status, age, citizenship, membership in protected classes, sexual orientation, disability, genetic information, familial or marital status, pregnancy, gender identity, gender reassignment, military or veteran status, or other protected characteristics, in accordance with applicable laws. Reasonable accommodations will be provided for known disabilities or chronic illnesses, unless undue hardship would occur.

For U.S.-based roles, salary ranges are provided in accordance with U.S. law. For roles in Japan and/or Canada, salaries are in accordance with local laws and currency. If outside these regions, please consult with your recruiter about salaries and benefits.

Background checks are part of the recruitment process, conducted according to the laws of the country where the position is based, to verify information such as identity, work rights, and educational qualifications.

Salary Range (annual): $92,500 - $151,100

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