Senior Statistical Programmer

This is a fully remote position, open to applicants in New Jersey.

📋 Description

• Create and delineate study data tabulation models and analysis data models for clinical trials, as well as for the integration of data from multiple trials, which includes ISS and ISE datasets.

• Produce comprehensive and efficient analysis data models in accordance with approved dataset designs or specifications.

• Conduct independent validation of datasets developed by other programmers or statisticians.

• Write SAS programming codes and generate complete and precise statistical output reports based on trial data.

• Perform independent validation of statistical output reports created by other programmers or statisticians.

• Develop and validate SAS codes for logical checks within clinical trial databases and reports to facilitate ongoing data review.

• Document data and programming details in compliance with corporate SOPs and guidelines.

• Archive clinical trial data and programming information following corporate archival SOPs and guidelines.

• Offer expertise in additional programming and system administration areas as needed.

• Provide technical support and guidance to junior Statistical Programmers.

• Participate in the continuous enhancement of statistical programming processes and protocols.

• Contribute to programming standards, conventions, and procedures within therapeutic areas as a lead programmer.

• Assist in the development of client-specific programming standards, conventions, and procedures as required.

⛳️ Requirements

• A Master’s degree in Mathematics or Statistics.

• A minimum of five years of experience.

• Proven experience in designing and specifying study data tabulation models and analysis data models for clinical trials or in integrating clinical trial data from multiple studies.

• Familiarity with common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor’s criteria.

• Competence in generating analysis data models in line with approved dataset designs or specifications.

• Capability to perform independent validation of datasets and statistical output reports.

• Expertise in SAS programming.

• Proficiency in developing and testing SAS codes for logical checks in clinical trial databases and reports.

• Understanding of corporate SOPs, guidelines, and archival SOPs.

• Ability to mentor and provide technical assistance to less experienced Statistical Programmers.

🏝️ Benefits

• Medical coverage.

• Dental coverage.

• Vision coverage.

• Life and AD&D insurance.

• Short-term disability.

• Long-term disability.

• Tuition reimbursement.

• Fitness reimbursement.

• Employee assistance program (EAP).

• 401(k) retirement plan.

• Generous paid time off.

• Sick leave.

• Opportunity to earn a performance-based bonus.