Senior Statistical Analyst I - Tigermed

Bilinguallink; Dartmouth; On-site; CAD 70,000 - 110,000; Full time

Job summary

Bilinguallink in Dartmouth, NS, is seeking a seasoned SAS Programmer to develop and validate complex analysis datasets (ADaM) and TFLs using SAS, write specs, and mentor junior team members. You will lead programming projects, manage timelines, communicate with clients as the primary programming contact, ensure quality through code review, and maintain compliance with ICH-GCP and CDISC standards.

This on-site role requires collaboration with global teams and contributes to regulatory

Qualifications

• Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field.
• 3+ years of SAS programming experience in pharmaceutical or CRO environments.
• Strong knowledge of clinical trials, statistical methods, and regulatory requirements.
• Proven experience leading programming projects and mentoring team members.
• Excellent communication skills and experience working with global teams and clients.
• Proficient in Microsoft Office and SAS software.

Responsibilities

• Develop and validate complex analysis datasets (ADaM) and TFLs using SAS.
• Write and review programming specifications and supporting documentation.
• Create standard macros and tools to improve efficiency.
• Serve as a project lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members.
• Communicate with clients as the key programming contact, including delivering outputs and managing feedback.
• Conduct SAS code review, track issues, and ensure quality standards are met.
• Archive all programming deliverables and documentation per SOPs.
• Mentor team members and support their technical and professional development.
• Ensure compliance with ICH-GCP, CDISC standards, and company SOPs.

Skills

SAS programming

CDISC

ICH-GCP

Clinical trials

Leadership

Communication

Education

Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field

Tools

SAS software

Microsoft Office

Job description

Key Responsibilities

• Develop and validate complex analysis datasets (ADaM) and TFLs using SAS.


• Write and review programming specifications and supporting documentation.


• Create standard macros and tools to improve efficiency.


• Serve as a project lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members.


• Communicate with clients as the key programming contact, including delivering outputs and managing feedback.


• Conduct SAS code review, track issues, and ensure quality standards are met.


• Archive all programming deliverables and documentation per SOPs.


• Mentor team members and support their technical and professional development.


• Ensure compliance with ICH-GCP, CDISC standards, and company SOPs.

Requirements

• Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field.


• 3+ years of SAS programming experience in pharmaceutical or CRO environments.


• Strong knowledge of clinical trials, statistical methods, and regulatory requirements.


• Proven experience leading programming projects and mentoring team members.


• Excellent communication skills and experience working with global teams and clients.


• Proficient in Microsoft Office and SAS software.