Referso Jobs

Senior Quantitative Modeler

Guidehouse · Posted Nov 12, 2026

Open

McLean, Virginia, United States
Senior
$130K–$216K per year
5–7 years

Apply with Referso

Senior Quantitative Modeler

Guidehouse · Posted Nov 12, 2026

Open

McLean, Virginia, United States
Senior
$130K–$216K per year
5–7 years

Apply with Referso

Senior Director, Biostatistics

Keros Therapeutics · Posted Nov 12, 2026

Open

Lexington, Massachusetts, United States
Hybrid
Full-time · Director
$264K–$303K per year
10+ years

Apply with RefersoAI Apply on careers page

This person will head the biostatistics function at Keros Therapeutics. The ideal candidate is a leader with a growth mindset. They will serve as the core internal statistical authority, doing heavy hands-on work at the program/study level while partnering closely with the Head of Biometrics to oversee consultants and CRO vendors.

Compensation

Potential base pay range $264,000—$303,000 USD

Responsibilities

Lead the biostatistics function, including managing current consultants, overseeing CRO vendors, and eventually recruiting, developing, and retaining top internal talent as the team scales
Lead the development and delivery of statistical methodology, biostatistical subject matter expertise, and statistical tools/applications development to support the development and marketing of new medicines
Partner with key stakeholders and functions including clinical data management to ensure the timely delivery of high-quality statistical support to clinical programs
Collaborate with other functions to ensure that advanced statistical expertise is appropriately integrated into clinical decision-making
Oversee the performance of project team members and consultants, ensuring a proper level of scientific rigor, effective team operation, and seamless cross-functional collaboration

Requirements

PhD in Statistics, Biostatistics, or equivalent
MS in Statistics, Biostatistics
Nice to have: R

Skills

Senior Scientist, Statistical Programming - SDTM

MSD · Posted Nov 10, 2026

Open

Pennsylvania, United States
Hybrid
Full-time · Senior
$117K–$184K per year
5+ years

Apply with RefersoAI Apply on careers page

Senior Statistical Programmer overseeing submission data standards quality management for global drug and vaccine regulatory submissions.

Compensation

$117,000.00 - $184,200.00

Responsibilities

Provide oversight and quality management of submission data standard deliverables
Plan and coach project teams on submission data standards
Consult with external vendors and partners
Maintain current knowledge of SDTM, ADaM, and other CDISC standards
Improve electronic submission processes and provide tools and templates

Requirements

BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field
Nice to have: R programming
Nice to have: Python programming
Nice to have: reporting processes

Skills

SAS programming CDISC SDTM CDISC ADaM Define.XML cSDRG

Summer 2027 - EVAAS Education Policy Graduate Intern

SAS · Posted Nov 10, 2026

Open

Cary, North Carolina, United States
Hybrid
Internship · Intern
$29–$49 per hour

Apply with RefersoAI Apply on careers page

Internship focused on developing policy briefs, research papers, and technical documentation for the EVAAS education analytics solution.

Compensation

Hourly rates for SAS internships are based on an applicant’s year in school and the role they are hired into. Rates range from $15 to $30 per hour for associate and bachelor’s-level positions and from $29 to $49 per hour for master’s and Ph.D positions.

Responsibilities

Support the development of policy briefs, research papers, and technical documentation
Analyze outcomes-based data and summarize results for internal and external stakeholders
Monitor education policy news and research in relevant areas
Document internal processes and strategies

Requirements

Master’s program
Nice to have: background in education, assessments, government, or policy

Skills

data analysis policy research technical writing communication mathematical documentation SAS programming

Senior Biostatistician

Travere Therapeutics · Posted Nov 6, 2026

Open

San Diego, California, United States
Hybrid
Full-time · Senior
$116K–$151K per year
2+ years

Apply with RefersoAI Apply on careers page

The Senior Biostatistician will work closely with the Biometrics Team lead to provide statistical support for assigned clinical studies. This role contributes to study design, statistical analysis, reporting, and interpretation of clinical trial data under the guidance of more senior statisticians.

Compensation

Target Base Pay Range: $116,000.00 - $151,000.00

Responsibilities

Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership
Collaborate with clinical, data management, statistical programming, and other cross-functional team members to support study activities
Contribute statistical input to study design, protocol development, endpoint definition, and analysis planning
Prepare and review assigned statistical analysis plans, case report forms, clinical database specifications, validation plans, table, figure, and listing shells, analysis dataset specifications, and related documentation
Perform statistical analyses, simulations, and ad hoc analyses as needed

Requirements

Master's degree in Statistics, Biostatistics, or related field
Ph.D. (preferred)
Nice to have: R or other statistical software
Nice to have: Experience working with external vendors or contract research organizations

Skills

Statistical principles and methods for clinical trials

Biostatistical Programming Manager

Lifelancer · Posted Jan 1, 2024

Open

Washington D.C., District of Columbia, United States
Full-time · Manager
$120K–$180K per year
2–10 years

Apply with RefersoAI Apply on careers page

In this vital role you will report to a Sr. Manager in CfOR’s Data & Analytic Center. This role will support the CfOR organization by setting goals with CfOR epidemiologists, laying out a strategy to deliver on those goals, and coordinating with a functional service provider (FSP)-based team of contract programmers to achieve the goals.

Compensation

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted.

Responsibilities

Lead an FSP-based programming team conducting analyses supporting CfOR’s Data & Analytic Center
Coordinate with functional leads to prioritize and manage workflow
Identify potential efficiency improvements and propose solutions
Collaborate with CfOR FSP liaison to ensure performance and quality standards from FSP-based programming team
Ensure the analysis and presentation of biomedical data is accurate and complete

Requirements

Doctorate degree
Master’s degree
Bachelor’s degree
Associate’s degree
High school diploma / GED

Skills

SAS programming R SQL Python Survival analysis

Associate Director, Statistical Programming

Celldex Therapeutics · Posted Nov 6, 2026

Open

Needham, Massachusetts, United States
Full-time · Director
$154K–$200K per year
8+ years

Apply with RefersoAI Apply on careers page

A senior-level leadership position focused on overseeing the end-to-end statistical programming lifecycle, combining technical oversight, project management, and cross-functional collaboration.

Compensation

The expected base salary for this position is: $153616.00 to $199501.00. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market. Subject to eligibility and applicable plan terms, compensation includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days.

Responsibilities

Lead or Co-ordinate statistical programming activities of all programmers either internally or externally assigned to the study/project work
mentor other programmers in functional expertise and processes
Make statistical programming decisions/recommendations at study or project level
Comply with company, department and industry standards (e.g. CDISC) and processes
responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results

Requirements

MS in Statistics or related field
Nice to have: R

Skills

SAS programming biotech/pharma industry experience

SAS Programming jobs

Compensation

Responsibilities

Requirements

Skills

Benefits

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits

Benefits

Benefits

Benefits