Associate Director, Statistical Programming

Verastem Oncology

Associate Director leading statistical programming and development of SAS programs for clinical studies. Overseeing quality assurance and collaboration with teams to meet regulatory requirements in a hybrid work environment.

Posted 6/17/2026full-timeNeedham • Massachusetts • 🇺🇸 United StatesSenior💰 $165,000 - $190,000 per yearWebsite

About the role

Key responsibilities & impact

Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the generation of tables, figures and listings for clinical study report(s), FDA submission(s), and medical congress abstracts/posters/presentations;
Responsible for internal statistical programming deliveries across multiple clinical studies, as well as implementing process improvements and department initiatives;
Identify areas within clinical development functions where statistical programming tools and applications can enhance processes;
Perform quality control checks of advanced SAS code and output produced by other statistical programmers;
Work closely with clinical operations, data management and statisticians to develop infrastructure for timely and quality reporting of clinical trials to support regulatory requirements, and product launch activities;
Proactively identify issues and recommend solutions to optimize preparation, execution, reporting, and documentation of statistical programming activities;
Provide project management and technical guidance to ensure operational and technical excellence;
Liaise with vendors as needed to facilitate electronic data transfers and statistical programming support.

Requirements

What you’ll need

Requirements include a Bachelor’s or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus nine years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries; or in the alternative, a Master’s degree or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus seven years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries.
If qualifying with bachelor’s degree, must have the following: 9 years of experience with SAS programing; 9 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS; 7 years of experience with CDISC SDTM and ADaM; 7 years of experience with electronic FDA submission; and 9 years of experience working in a clinical trial setting.
If qualifying with Master’s degree, must have the following: 7 years of experience with SAS programing; 7 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS; 5 years of experience with CDISC SDTM and ADaM; 5 years of experience with electronic FDA submission; and 7 years of experience working in a clinical trial setting.

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Verastem Oncology Website LinkedIn All Job Openings 51 - 200 employees Founded 2010 🧬 Biotechnology 💊 Pharmaceuticals Biotechnology
Pharmaceuticals Verastem Oncology is a clinical-stage biopharmaceutical company focused on developing novel small-molecule therapies that target the RAS/MAPK signaling pathway to treat aggressive and recurrent cancers. The company develops and advances combination therapies, including RAF/MEK clamp and FAK inhibitors (e. g. , avutometinib and defactinib), and has an FDA-approved combination for KRAS-mutant recurrent low-grade serous ovarian cancer. Verastem runs multiple clinical trials, collaborates strategically, and centers its pipeline on inhibiting RAS-driven tumor biology to improve patient outcomes. Associate Director, Statistical Programming Job not on LinkedIn 🔥 36 minutes ago 🏢🏡 Needham – Hybrid 💵 $165k - $190k / year ⏰ Full Time 🟠 Senior 👔 Director 🦅 H1B Visa Sponsor Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the generation of tables, figures and listings for clinical study report(s), FDA submission(s), and medical congress abstracts/posters/presentations;
Responsible for internal statistical programming deliveries across multiple clinical studies, as well as implementing process improvements and department initiatives;
Identify areas within clinical development functions where statistical programming tools and applications can enhance processes;
Perform quality control checks of advanced SAS code and output produced by other statistical programmers;
Work closely with clinical operations, data management and statisticians to develop infrastructure for timely and quality reporting of clinical trials to support regulatory requirements, and product launch activities;
Proactively identify issues and recommend solutions to optimize preparation, execution, reporting, and documentation of statistical programming activities;
Provide project management and technical guidance to ensure operational and technical excellence;
Liaise with vendors as needed to facilitate electronic data transfers and statistical programming support. 🎯 Requirements
Requirements include a Bachelor’s or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus nine years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries; or in the alternative, a Master’s degree or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus seven years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries.
If qualifying with bachelor’s degree, must have the following: 9 years of experience with SAS programing; 9 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS; 7 years of experience with CDISC SDTM and ADaM; 7 years of experience with electronic FDA submission; and 9 years of experience working in a clinical trial setting.
If qualifying with Master’s degree, must have the following: 7 years of experience with SAS programing; 7 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS; 5 years of experience with CDISC SDTM and ADaM; 5 years of experience with electronic FDA submission; and 7 years of experience working in a clinical trial setting. Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

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Hard Skills & Tools

SAS programmingBASE/SASSAS/STATSAS/GRAPHSAS MACROSCDISC SDTMCDISC ADaMelectronic FDA submissionstatistical programmingquality control

Soft Skills

project managementtechnical guidanceproblem-solvingcommunicationcollaboration