Principal Statistical Programmer

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

📋 Description

• Oversee projects that present a higher degree of complexity, challenges, and difficulties.

• Drive initiatives to address complicated statistical programming issues or obstacles.

• Assume a leadership position in statistical programming projects.

• Support statistical programming management in effectively planning and distributing resources.

• Engage in the development and maintenance of standards for clinical trial data and statistical programming.

• Conduct primary statistical programming and validation programming hands-on for assigned projects.

• Develop SDTM mapping specifications and ADaM data specifications.

• Carry out quality control (QC) reviews of documents prepared by others.

• Generate SDTM and ADaM define.xml files.

• Offer training, mentorship, and technical support to less experienced Statistical Programmers.

⛳️ Requirements

• M.Sc., M.A., or an equivalent higher degree in Statistics, Biostatistics, Computer Science, or related fields.

• 10 years of relevant experience with M.Sc. or M.A. / 9 years with a Ph.D.

• Comprehensive knowledge of clinical trial data processing and manipulation.

• Practical experience in statistical programming and analysis.

• Familiarity with industry standards.

• Understanding of regulatory and ICH requirements.

• Proficiency in SAS programming.

• Deep insight into data standardization.

• Strong leadership skills and a commitment to achieving objectives.

🏝️ Benefits

• Medical, dental, and vision coverage.

• Life & AD&D insurance.

• Short- and long-term disability benefits.

• Tuition reimbursement.

• Fitness reimbursement.

• Employee assistance program (EAP).

• A 401(k) retirement plan.

• Generous paid time off and sick leave.

• Opportunity to earn a performance-based bonus.