Referso Jobs

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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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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BSI DO Data analist

belastingd · Posted Nov 9, 2026

Open

Apeldoorn, Gelderland, Netherlands +1 more
Full-time

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Data analyst in the Central Administrative Processes division, focusing on debt collection and payment flows, operating in Apeldoorn and supporting the cluster Inning.

Locations (2)

Apeldoorn, Gelderland, Netherlands
Netherlands

Responsibilities

Select and analyze data
Provide reliable advice to management
Translate findings into concrete proposals
Initiate research on trends and developments
Analyze data models

Requirements

Bachelor's in Computer Science, Business Administration or comparable
Nice to have: Knowledge of debt collection and payment flows

Skills

SAS Base DB2 SAS Viya

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

Associate Director, Statistical Programming

Celldex Therapeutics · Posted Nov 6, 2026

Open

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

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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

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

Credit Collections Reporting Analyst

NRG Energy, Inc. · Posted Nov 6, 2026

Open

Edmonton, Alberta, Canada
3+ years

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The Credit/Collections Reporting Analyst delivers analytical support for Direct Energy’s active and inactive credit and debt portfolios, assessing credit risk strategies, portfolio results, dunning effectiveness, and bad debt trends to inform operational and strategic decisions.

Responsibilities

Develop and maintain performance reporting for active and inactive portfolios
Track credit risk, delinquency, and bad debt trends
Create dashboards, scorecards, and operational reports
Deliver variance analysis and actionable performance insights
Support portfolio forecasting and modelling

Requirements

Bachelor’s degree in Business Analytics, Data Science, Computer Science, or a related field from an accredited four-year institution
Two-year diploma combined with relevant work experience may also be considered
Nice to have: Experience in the utility or energy industry
Nice to have: Collections or bad debt analysis experience
Nice to have: Vendor performance reporting experience

Skills

Advanced Microsoft Power BI DAX Power Query data modelling

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

Biostatistical Programming Sr Mgr

Amgen · Posted Nov 5, 2026

Open

Remote, United States
Remote
Senior
$152K–$205K per year
8+ years

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Lead and manage biostatistical programming activities for Amgen’s Biosimilar organization, coordinating with CROs and cross‑functional teams to develop datasets, analysis plans, and submission packages.

Compensation

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Salary Range 151,838.05USD -205,427.95 USD

Responsibilities

Represent the product programming function and participate in multidisciplinary project team meetings
Collaborate closely with Biosimilar Statisticians and other functional team members
Coordinate and oversee the development of dataset specifications and implementation of TLGs according to the statistical analysis plans
Review and approve analysis dataset specifications
Review or contribute to data management plans, database development, and edit checks plan

Requirements

BA/BSc or higher degree in quantitative or scientific subjects
Nice to have: MSc or higher degree in quantitative or scientific subjects
Nice to have: Java
Nice to have: R
Nice to have: Regulatory submissions experience

Skills

Advanced SAS programming SAS BASE

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