Referso Jobs

Director, Statistical Programming

X4 Pharmaceuticals INC · Posted Nov 10, 2026

Open

Boston, Massachusetts, United States
Manager
8+ years

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Director, Statistical Programming

X4 Pharmaceuticals INC · Posted Nov 10, 2026

Open

Boston, Massachusetts, United States
Manager
8+ years

Apply with Referso

Spec 3, Statistics & Statistics Programming

Mindlance · Posted Nov 6, 2026

Open

Irvine, California, United States
On-site
Contract · Senior
6+ years

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Provide hands‑on statistical programming support for clinical studies, developing and validating analysis datasets, tables, listings, figures, and graphs for regulatory submissions and internal presentations.

Compensation

Bill Rate is *** On Site or Remote Provide hands‐on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company standards.

Responsibilities

Develop complex analysis datasets, specifications, and summary outputs
Create, modify, and maintain SAS programs
Perform independent program review and validation
Support ad hoc and planned analyses
Partner with Clinical Data Management and Biostatistics

Requirements

Bachelor’s degree in Statistics, Mathematics, Computer Science, or a related field
Master’s degree (or equivalent) in a related field
Nice to have: R
Nice to have: Python
Nice to have: Experience with regulatory submissions

Skills

SAS Base SAS/STAT SAS Macros CDISC standards (SDTM, ADaM)Regulatory requirements (GCP, ICH, FDA, ISO)

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

Associate Director, SAS Programming

Acadia Pharmaceuticals Inc. · Posted Nov 6, 2026

Open

Remote, United States
Remote
Full-time · Manager
$163K–$203K per year
8+ years

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Lead statistical programming for assigned compounds, ensuring quality, CDISC conformance, and submission readiness.

Compensation

$162,600—$203,300 USD

Responsibilities

Serve as programming lead for assigned compound
Set programming strategy and standards
Develop and maintain resource plans
Provide input into analysis plans and CRFs
Perform hands‑on development and validation of SDTM, ADaM, and TLF programs

Requirements

Bachelor's degree in statistics, biostatistics, computer science, mathematics, or related field
Master's degree preferred
Nice to have: SAS certification at the Advanced Programmer level
Nice to have: Experience with NDA/BLA submissions
Nice to have: Working knowledge of R

Skills

Expert-level SAS programming Base SAS SAS/STAT SAS Macro ODS SAS/GRAPH

Statistics & Statistics Programming - Specialist 3

Sunrise Systems Inc · Posted Nov 6, 2026

Open

Irvine, California, United States
On-site
Contract · Senior
$75–$78 per hour
8+ years

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Provide hands‑on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs.

Compensation

Compensation: The hourly rate for this position is between $75.00-$78.00 per hour.

Responsibilities

Develop complex analysis datasets, specifications, and summary outputs for inclusion in clinical study reports, regulatory submissions, and internal presentations.
Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure efficient programming, reporting, review, and traceability.
Perform independent program review and validation, ensuring complete, accurate, and inspection‑ready documentation in compliance with applicable regulations and internal procedures.
Support ad hoc and planned analyses in collaboration with the designated statistician, including responses to data review questions.
Partner with Clinical Data Management and Biostatistics to review CRFs, database specifications, edit checks, and data derivations as needed.

Requirements

Bachelor’s degree in Statistics, Mathematics, Computer Science, or a related field
Master’s degree (or equivalent) in a related field
Nice to have: Python
Nice to have: R

Skills

SAS Base

M10912 產品機構工程師

WNC Corporation (formerly Wistron NeWeb Corporation) · Posted Jul 27, 2026

Open

Hsinchu, Taiwan, Taiwan

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Responsibilities

主導現場異常分析並追蹤改善
執行CPK分析、TPI申請、WE改善
優化制程SOP與人因錯誤點防呆
撰寫PFMEA與Control Plan基本框架
協助治具開發驗證並撰寫報告

Skills

Advanced Interactive Multidimensional Modeling System (AIMMS)Analysis of Variance (ANOVA)Crystal Reports (Reporting Software)Database Analysis Mathematical Analysis Mathematical Programming MAXQDA Microsoft Power Platform SAS/STAT AIMMS ANOVA Crystal Reports

Director, Statistical Programming

Director, Statistical Programming

Responsibilities

Requirements

Skills

Spec 3, Statistics & Statistics Programming

Compensation

Responsibilities

Requirements

Skills

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

Responsibilities

Requirements

Skills

Associate Director, SAS Programming

Compensation

Responsibilities

Requirements

Skills

Statistics & Statistics Programming - Specialist 3

Compensation

Responsibilities

Requirements

Skills

M10912 產品機構工程師

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Skills

Benefits

Benefits

SAS/STAT jobs

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Requirements

Skills

Compensation

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Skills

Responsibilities

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Skills

Compensation

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Compensation

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