Senior Statistical Programmer

Connect Life Sciences; New York (NY); Remote; USD 90,000 - 250,000; Full time

Job summary

An established industry player is seeking a Senior Recruiter and Writer to join their innovative team. This remote position emphasizes the importance of statistical programming and data analysis in clinical trials. You will leverage your expertise in SAS programming to design data models and ensure the integrity of trial data. Collaborating with a talented team, you will contribute to the continuous improvement of programming processes while mentoring less experienced colleagues. This role offers a unique opportunity to impact the pharmaceutical and biotechnology sectors significantly.

Qualifications

• Master's Degree in Statistics or Biostatistics, with at least five years experience.
• Experience in clinical trial data management and statistical programming.

Responsibilities

• Design and specify study data tabulation models for clinical trials.
• Generate complete analysis data models and validate datasets.
• Develop SAS codes for statistical output reports and logical checks.

Skills

SAS Programming

Statistical Analysis

Data Validation

Clinical Trial Data Management

Programming Documentation

Education

Master's Degree in Statistics or Biostatistics

Tools

SAS

Job description

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Senior Recruiter at Connect Life Sciences & Writer

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Qualifications And Experience

• Master's Degree in Statistics or Biostatistics, with at least five years experience.

Responsibilities:

• Design and specify study data tabulation models and analysis data models for clinical trials or for the integration of clinical trial data from multiple trials (e.g. ISS and ISE datasets). These designs and specifications are completed in accordance with common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor’s requirements.
• Generate complete and efficient analysis data models following approved dataset designs or specifications. Perform independent validation of datasets created by other programmers or statisticians.
• Develop SAS programming codes and generate complete and accurate statistical output reports of trial data in well-defined formats.
• Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers or statisticians.
• Develop and test SAS codes for clinical trial database logical checks and reports for ongoing data review.
• Document data and programming information in accordance with corporate SOPs and guidelines.
• Archive clinical trial data (study data tabulation models and analysis data models) and programming information in accordance with corporate archival SOPs and guidelines.
• Develop and provide expertise in other programming and system administration areas when required.
• Provide technical guidance and support to less experienced Statistical Programmers.
• Contribute to the continuous improvement of the statistical programming processes and procedures.
• Contribute to the establishment of therapeutic area programming standards/conventions/procedures within assigned therapeutic areas as a lead programmer.
• Contribute to the establishment of client specific programming standards/conventions/procedures for assigned clients when required.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Analyst, Health Care Provider, and Research

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Research Services

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