Position Details

Type Full-Time

Experience mid

Exp. Years 5+ years

Education Bachelor's degree required

Category Data & Analytics

About this role

Senior statistical programmer leading SAS-based programming for clinical trials, delivering analysis datasets, tables, listings, and figures to meet CDISC standards and regulatory guidelines.

Key Responsibilities

Lead statistical programming activities; author ADaM datasets and endpoints; manage end-to-end programming from CRF to submissions; ensure regulatory standards; vendor oversight

Technical Overview

Focus on SAS programming across Base/STAT/GRAPH/MACRO, with CDISC/ADaM, UNIX, and R; familiarity with imaging/genomics software and regulatory submissions.

Ideal Candidate

Ideal candidate is a senior statistical programmer with 5+ years of SAS experience, CDISC/ADaM expertise, and strong clinical trial background. The candidate should be proficient in UNIX, R, and have familiarity with imaging/genomics software and regulatory guidelines (ICH/FDA/EMEA/ROW).

Must-Have Skills

Bachelor's degree5+ years SAS Base programming5+ years SAS STATGRAPHand MACRO5+ years clinical trial experience3+ years clinical database experienceCDISC and/or submissions experienceKnowledge of drug development process and clinical trialsKnowledge of drug submission requirements (ICHFDA/EMEA/ROW)UNIX familiarity

Nice-to-Have Skills

Familiarity with AI and ML concepts

Required Skills

SAS Base programmingSAS STATSAS GRAPHSAS MACROCDISCADaMUNIXRImaging softwareGenomics softwareCDISC/submissions experiencedrug development processregulatory guidelines

Hard Skills

SAS Base programmingSAS STATSAS GRAPHSAS MACROCDISCADaMUNIXRImaging softwareGenomics softwareCDISC/submissions experienceDrug development processICH FDA/EMEA/ROW guidelinesUNIX familiarity

Soft Skills

Attention to detailCommunicationAbility to manage competing prioritiesTeam collaborationLeadership

Industry & Role

Industry Healthcare & Medical

Job Function Lead statistical programming activities and ensure regulatory-compliant, submission-ready outputs for clinical studies.

Role Subtype Senior statistical programmer

Keywords for Your Resume

statistical programmersenior analystclinical trialssas base programmingsas statsas graphsas macrocdiscadamunixrcdisc/submissions experiencedrug developmentich guidelinesfda eme a row guidelinesunIX familiarityclinical database experiencecdisc adamsimaging softwaregenomics softwarecdisc submissions

Deal Breakers

Lack of SAS experience or clinical trial experience, No CDISC/ADaM or submission experience

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