Senior Statistical Programmer

Cytel - USA & APAC; Cambridge (MA); Remote; USD 99,000 - 149,000; Full time

Job summary

A leading company in the Pharmaceutical industry is seeking a Senior Statistical Programmer to lead statistical programming projects. The role involves ensuring compliance with regulatory requirements and mentoring staff on SAS techniques. Candidates should have a degree in Statistics or related field and significant experience in biostatistics.

Qualifications

• Bachelor's degree in Statistics, Health Informatics, Biochemistry, or related field.
• 6 years of experience in biostatistics/statistical programming.
• 2 years of SAS programming experience.

Responsibilities

• Lead and contribute to statistical programming projects.
• Ensure compliance with regulatory requirements.
• Provide training on SAS techniques and clinical trial data.

Skills

SAS programming

CDISC ADaM

CDISC SDTM

Statistical analysis

Project management

Education

Bachelor's degree in Statistics

Master's degree in Statistics

Job description

JOB DESCRIPTION

Notice of Filing of Application for Permanent Employment Certification

This notice is being posted in connection with and as a result of the filing of an application for permanent alien labor certification for the below-described job opportunity. Any person may provide documentary evidence bearing on the application, with information on available workers or information on wages and working conditions, to a Certifying Officer of the U.S. Department of Labor, whose address is as follows: Certifying Officer, U.S. Department of Labor, Employment and Training Administrator, Office of Foreign Labor Certification, 200 Constitution Avenue NW, Room N-5311, Washington, D.C. 20210.

Information about the Job Opportunity

Employer Name : Cytel Inc.

Job Location : 675 Massachusetts Ave., Cambridge, MA 02139

Job Title : Senior Statistical Programmers

Job Duties : Work directly with stakeholders to lead and contribute to statistical programming projects and to ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements. Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results. Provide relevant training and mentorship to staff and project teams on SAS techniques and clinical trial data with respect to CDISC standards and other regulatory requirements. 100% telecommuting. Salary range: $99,200 - $148,800 per year.

Minimum Requirements : Bachelor's degree in Statistics, Health Informatics, Biochemistry, or a closely related field and 6 years of experience in biostatistics or statistical programming activities in the Pharmaceutical or Biotechnology industry in clinical development, including: 2 years of experience in SAS programming; 2 years of experience with CDISC ADaM and SDTM, ICH Statistical, and Clinical Report guidelines; and 1 year of experience as lead statistical programmer working with global cross functional teams to include project management.

Will also accept a Master's degree in Statistics, Health Informatics, Biochemistry, or a closely related field and 3 years of experience in biostatistics or statistical programming activities in the Pharmaceutical or Biotechnology industry in clinical development, including: 2 years of experience in SAS programming; 2 years of experience with CDISC ADaM and SDTM, ICH Statistical, and Clinical Report guidelines; and 1 year of experience as lead statistical programmer working with global cross functional teams to include project management.

Interested candidates may contact Jayne Stegman, [e-mail] with job ID 724 in subject line.