Referso Jobs

Statistical programmer

Zealand Pharma A/S · Posted Oct 6, 2025

Open

Copenhagen, Capital Region, Denmark
5+ years

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Statistical programmer

Zealand Pharma A/S · Posted Oct 6, 2025

Open

Copenhagen, Capital Region, Denmark
5+ years

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Senior Biostatistician

Travere Therapeutics · Posted Nov 6, 2026

Open

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

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Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership.

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 with external vendors or contract research organizations

Skills

statistical support

Biostatistics Director- Global BIOS

IQVIA · Posted Nov 6, 2026

Open

Durham, North Carolina, United States
Senior
$135K–$376K per year
11–13 years

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Lead statistical methodology for clinical trial design and provide high-level guidance to internal and external clients as a Director of Biostatistics.

Compensation

The potential base pay range for this role, when annualized, is $134,800.00 - $375,700.00.

Responsibilities

Lead statistical methodology for clinical trial design
Provide high-level guidance to internal and external clients
Specialize in at least one area of statistical leadership
Serve as subject matter expert
Fulfil general consulting roles

Requirements

PhD in Statistics or Biostatistics
MSc in Statistics or Biostatistics
Nice to have: teaching
Nice to have: publishing papers
Nice to have: presenting talks

Skills

clinical trial design adaptive design regulatory bodies FDA experience SAS CDISC SDTM

Principal Statistical Programmer

Emmes Group · Posted Nov 6, 2026

Open

Bengaluru, Karnataka, India
Principal
7–9 years

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A senior-level contributor responsible for designing, developing, validating, and maintaining statistical programming deliverables to support clinical trials and regulatory submissions.

Responsibilities

Lead the development, validation, and maintenance of SDTM and ADaM datasets and associated documentation.
Program complex Tables, Listings, and Figures (TLFs) for study reports, publications, and submissions.
Review and interpret statistical analysis plans (SAPs) to ensure accurate implementation in code.
Serve as lead programmer on multiple studies and/or projects, coordinating efforts across internal teams and CROs.
Provide technical oversight and mentoring to junior programmers and contractors.

Requirements

Bachelor's Degree
Master's degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field

Skills

SAS Base SAS Macro SAS SQL CDISC SDTM CDISC ADaM ICH GCP

Senior Manager, Statistical Programming

Eisai US · Posted Nov 6, 2026

Open

Remote
Remote
Full-time · Manager
$139K–$182K per year
8+ years

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Lead and manage statistical programming projects for clinical studies, ensuring quality deliverables and process improvement.

Compensation

The annual base salary range for the Senior Manager, Statistical Programming is from :$138,800-$182,200. Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan.

Responsibilities

Manage statistical programming projects
Develop and review SAS code and datasets
Create summary tables, graphs, and listings
Review statistical analysis plans
Collaborate with Biostatistics, Data Management, Clinical Ops

Requirements

Bachelor's in Computer Science
Bachelor's in Public Health
Bachelor's in Biostatistics
Bachelor's in Statistics
Master's in Computer Science

Skills

SAS CDISC SDTM CDISC ADaM Vendor Management Statistical Programming Project Management

Principal Statistical Programmer Consultant – Oncology (Solid Tumors)-Remote

ClinChoice · Posted Nov 6, 2026

Open

Remote, United States
Remote
Contract · Principal

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Lead and oversee statistical programming activities for oncology clinical trials, providing expertise and leadership in support of clinical development programs.

Responsibilities

Lead and oversee statistical programming activities for oncology clinical trials
Develop, validate, and maintain SDTM and ADaM datasets in compliance with CDISC standards
Program and review complex TFLs for clinical study reports and regulatory submissions
Support oncology efficacy and safety analyses
Demonstrate expertise in Kaplan-Meier analysis, Cox proportional hazards models, and other time-to-event analyses

Requirements

Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related discipline
Nice to have: Immuno-oncology
Nice to have: Targeted cancer therapies
Nice to have: Head and neck, lung, colorectal, breast solid tumor indications
Nice to have: FDA or EMA regulatory submissions

Skills

SAS programming SAS Base SAS Macro SAS/STAT CDISC SDTM

Senior Statistical Programmer FSP

Cytel Inc · Posted Nov 6, 2026

Open

Remote, India
Remote
Full-time · Senior
8+ years

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Senior Statistical Programmer supporting Phase I-IV clinical trials with SAS programming and CDISC standards, fully remote.

Responsibilities

Perform data manipulation, analysis and reporting of clinical trial data
Generate and validate SDTM and ADaM datasets and TLFs
Production and QC/validation programming
Generate complex ad-hoc reports
Apply efficacy analysis

Requirements

Bachelor’s degree in Statistics, Computer Science, Mathematics, or related field
Nice to have: Master’s degree or above
Nice to have: Study lead experience
Nice to have: Experience with immunology, respiratory or oncology studies

Skills

SAS programming CDISC SDTM CDISC ADaM Efficacy analysis QC/validation Ad-hoc reporting Clinical trial data manipulation

Biostatistics Director- Global BIOS

Lifelancer · Posted Nov 7, 2026

Open

Remote, Canada
Remote
Full-time
$135K–$376K per year
11–13 years

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Lead statistical methodology for clinical trial design and provide consulting to internal and external clients.

Compensation

The potential base pay range for this role, when annualized, is $134,800.00 - $375,700.00.

Responsibilities

Lead statistical methodology for clinical trial design
Provide high level guidance to internal and external clients
Serve as subject matter expert in statistical leadership
Manage multiple tasks and projects
Prepare budgets/proposals and participate in bid defences

Requirements

PhD or MSc degree in Statistics, Biostatistics, or related field

Skills

clinical trial design adaptive design biosimilars master protocols Bayesian analyses SAS CDISC SDTM CDISC ADaM

Senior Director/Executive Director, Biostatistics

Nkarta, Inc. · Posted Nov 1, 2026

Open

South San Francisco, California, United States
Hybrid
Full-time · Senior
$300K–$360K per year
8+ years

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Lead the biostatistics strategy for the NKX019 autoimmune program and serve as statistician of record across all indications, studies and health-authority interactions.

Compensation

$300,000—$360,000 USD

Responsibilities

Lead the biostatistics strategy for the NKX019 autoimmune program
Author and own statistical analysis plans (SAPs) and amendments
Independently perform complex analyses
Design potential pivotal studies, including power and sample-size justification
Translate the evolving Phase 1/2 dataset into the quantitative case for indication, dose and development decisions

Requirements

PhD in Biostatistics or Statistics
Nice to have: cell or gene therapy
Nice to have: B cell-directed therapies
Nice to have: patient-reported outcome instrument development
Nice to have: dose-escalation designs

Skills

SAS R CDISC SDTM CDISC ADaM statistical analysis

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