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 career 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 .

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📌 Senior Statistical Analyst I - Tigermed (Shubenacadie)
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📍 Shubenacadie