ZipRecruiter

Log In

1

Associate Sas Programmer Jobs in Wakefield, MA (NOW HIRING)

PepGen

Associate Director, Biostatistics

Boston, MA · On-site

$205K - $236K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Associate Director, Biostatistics will work in collaboration with the Head of Biometrics and ... Must have hands-on experience with SAS and R programming in clinical trials * Experience supporting ...

Vrtx

Biostatistics Associate Director (HYBRID)

Boston, MA · Hybrid

$174K - $262K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Collaborates with statistical programming and other functions to ensure timely delivery of TFLs ... In-depth competence with SAS and R statistical software * In-depth understanding of advanced ...

OSI

Associate Director, Biostatistics

Boston, MA · On-site

$205 - $236/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Associate Director, Biostatistics will work in collaboration with the Head of Biometrics and ... Must have hands-on experience with SAS and R programming in clinical trials * Experience supporting ...

New

Thinkbrg

2027 Summer Associate (Intern)

Boston, MA

$16.25 - $21.75/hr

... Stata,SAS,Python, or Snowflake. * Interact with senior staff,experts,and clients ... Experience with statistical, econometric and programming tools such as Excel, Stata, R, Python ...

Tufts Medicine

Research Associate I (Lab)

Boston, MA · On-site

... SAS, SPSS, or S-Plus. 4. Experience teaching statistics and statistical programming. Duties and Responsibilities: The duties and responsibilities listed below are intended to describe the general ...

ViziRecruiter,LLC.

Manager Advanced Analytics

Quincy, MA · On-site

$125.20 - $187.80/hr

Ahold Delhaize USA associates support the brands with a wide range of services, including Finance ... Extensive hands‑on experience using statistical programming software and languages such as SAS ...

Tror AI for everyone

Cloud/Platform Architect

Cambridge, MA · On-site

$70.75 - $93/hr

Architect Amazon EKS with namespace isolation (cdap/sas/gitlab) and Helm-based deployments ... Work with stakeholders (client, engineering, ops) to manage risks, dependencies, and design ...

previous page

Showing results 41-60

All JobsAssociate Sas Programmer JobsAssociate Sas Programmer Jobs in Wakefield, MA

Associate Sas Programmer information

See Wakefield, MA salary details

$15

$51

$83

How much do associate sas programmer jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for associate sas programmer in Wakefield, MA is $51.66, according to ZipRecruiter salary data. Most workers in this role earn between $36.25 and $64.86 per hour, depending on experience, location, and employer.

What is an Associate SAS Programmer?

An Associate SAS Programmer is an entry-level professional who specializes in using SAS (Statistical Analysis System) software to manage, analyze, and report data. They typically assist more senior programmers and statisticians in preparing datasets, writing code, and generating statistical reports, often within industries such as healthcare, finance, or research. This role requires a good understanding of SAS programming language, attention to detail, and the ability to follow standard operating procedures. Associate SAS Programmers often work as part of a larger data or analytics team, supporting projects by ensuring data integrity and accurate analyses.

What are the typical responsibilities of an Associate SAS Programmer?

As an Associate SAS Programmer in clinical research, you will primarily be responsible for writing and validating SAS programs to analyze clinical trial data, generate tables, listings, and figures, and ensure data integrity and compliance with regulatory standards. Your daily tasks may also include collaborating closely with statisticians, data managers, and senior programmers to review requirements and resolve data issues. This role often involves learning industry best practices and becoming familiar with CDISC standards, offering a strong foundation for career advancement in clinical data programming.

What are the key skills and qualifications needed to thrive as an Associate SAS Programmer?

To thrive as an Associate SAS Programmer, you need a solid understanding of statistical analysis, data management, and proficiency in SAS programming, often supported by a degree in statistics, computer science, or a related field. Familiarity with SAS software, data visualization tools, and knowledge of regulatory requirements or CDISC standards are typically expected, and SAS certification can be an advantage. Attention to detail, problem-solving ability, and effective communication are key soft skills for this role. These skills are crucial for ensuring accurate data analysis, efficient workflow, and clear reporting in data-driven environments such as clinical research or business analytics.

What job categories do people searching Associate Sas Programmer jobs in Wakefield, MA look for?

The top searched job categories for Associate Sas Programmer jobs in Wakefield, MA are:

What cities near Wakefield, MA are hiring for Associate Sas Programmer jobs?

Cities near Wakefield, MA with the most Associate Sas Programmer job openings:

Associate Sas Programmer jobs near you
Infographic showing various Associate Sas Programmer job openings in Wakefield, MA as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $107,455 per year, or $51.7 per hour.

Associate Director, Real World Evidence (RWE) Science

Ubertal Inc

Waltham, MA • Remote

Contractor

Re-posted 3 days ago

Job description

Job Title: Associate Director, Real World Evidence (RWE) Science – Phase IV / Post-Approval (Contract)

Location: United States (Remote; Eastern Time business hours preferred)
Duration: 7-Month Contract (Full-Time, 40 hours/week)
Start: Targeting Early March 2026

We are seeking an experienced Associate Director, Real World Evidence (RWE) Science to provide coverage for a Phase IV / post-approval RWE portfolio within a global Medical Affairs environment. This is a senior-level individual contributor role requiring deep epidemiology and real-world evidence expertise, strong methodological leadership, and the ability to independently manage ongoing studies with minimal ramp-up.

This position supports global stakeholders, including Europe, and requires flexibility for early morning meetings aligned to EU collaboration.

Key Responsibilities

  • Lead scientific oversight of Phase IV and post-approval real-world evidence (RWE) and observational studies

  • Provide methodological and technical leadership for study design, feasibility assessments, and evidence planning (EU focus)

  • Oversee vendors/CROs conducting outsourced analyses; review protocols, statistical analysis plans, and outputs to ensure scientific rigor

  • Conduct and/or supervise systematic literature reviews (SLRs) and meta-analyses

  • Contribute to development of RWE plans aligned with regulatory, HTA, and post-approval commitments

  • Support retrospective analyses leveraging real-world data sources (claims, EHR, registries)

  • Guide protocol development for observational studies and pragmatic trials

  • Perform evidence reviews to inform regulatory submissions, reimbursement strategy, and medical strategy

  • Collaborate with Regional Medical Affairs on scientific exchange and external RWE engagement

  • Support development of abstracts, posters, manuscripts, and internal scientific communications

Required Qualifications

  • Advanced degree (MD, PhD, or MS) in Epidemiology, Biostatistics, Public Health, or related field

  • 8–10+ years of progressive experience in epidemiology and real-world evidence

  • Minimum 5 years of Pharma or Biotech industry experience

  • Strong expertise in:

    • Phase IV / post-approval epidemiologic study design

    • Retrospective real-world data (RWD) analyses

    • Observational research methodologies

  • Experience overseeing vendors/CROs and critically evaluating statistical methodologies

  • Proficiency with statistical software (R, SAS, Stata) and strong understanding of claims/EHR data structures

  • Demonstrated ability to work autonomously in a global, matrixed environment

  • Flexibility to support EU collaboration across time zones

Preferred Qualifications

  • Experience supporting regulatory or HTA-facing RWE deliverables

  • Vaccines, infectious disease, or public health epidemiology background

  • Experience with systematic literature reviews and meta-analyses

  • R programming skills, including simulations, power calculations, or Shiny applications

  • Experience with data extraction, cleaning, and standardization for RWD

  • Prior authorship of scientific publications and presentations

  • Experience supporting EU feasibility assessments and RWE expectations

Role Highlights

  • Senior-level RWE leadership without people management responsibilities

  • High-visibility Phase IV and real-world effectiveness portfolio

  • Global collaboration with strong EU engagement

  • Remote flexibility within the United States

Qualified candidates with deep RWE and epidemiology expertise, strong methodological grounding, and Phase IV experience in Pharma/Biotech are encouraged to apply.