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Statistical programmer • durham nc

Last updated: 1 day ago

SAS Programmer III

Katalyst HealthCares & Life SciencesDurham, NC
Full-time

Review and ensure accurate and high-quality statistical programming deliverables from CRO.Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and gu...Show more

Associate Director, Specialist Programmer

AstraZenecaDurham, NC, US
Full-time

Type: Hybrid (3 days in office + 2 days from home).AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescrip...Show more

Quality Engineer

The Fountain GroupDurham, NC
Full-time

Reporting directly to the Quality Engineering Supervisor, this position involves product team support for the manufacturing operations, provides quality guidance, product resolution decisions, and ...Show more

Principal Biostatistician FSP, Late Phase

IQVIADurham, North Carolina, US
Full-time +1

Job Level: FSP Principal Biostatistician, Late Phase.Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Ser...Show more

Biostatistician II

Duke HealthDurham, NC, US
Full-time

Work Arrangement: On-Site Requisition Number: 268462 Regular or Temporary: Regular Location:.Personnel Area: MEDICAL CENTER Date: Mar 31, 2026 School of Medicine Established in 1930, Duke Universit...Show more

Principal Statistical Programmer, R Programming

IQVIADurham, North Carolina, US
Full-time +1

The Statistical Programmer is a key contributor to the research team, playing a crucial role in analyzing and interpreting complex data sets.They are responsible for developing and implementing sta...Show more

Mammography Technologist - Part Time

Duke HealthDurham, North Carolina, United States
Part-time

At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community.No matter where your talents lie, join us and disc...Show more

 • Promoted

Senior Biostatistician FSP, Late Phase

IQVIADurham, North Carolina, US
Full-time +1

Posting Title- R1539879 Senior Biostatistician FSP, Late Phase.Job Level: FSP Senior Biostatistician, Late Phase.Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our spo...Show more

Senior Clinical Programmer

IQVIADurham, North Carolina, US
Full-time +1

This Clinical Programmer role at IQVIA supports Risk‑Based Quality Management by developing and validating KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring platform.The p...Show more

ASSOCIATE DIRECTOR, BIOSTATISTICS DCRI

Duke HealthDurham, NC, US
Full-time

ASSOCIATE DIRECTOR, BIOSTATISTICS DCRI.Work Arrangement: Requisition Number: 265691 Regular or Temporary: Regular Location:.Personnel Area: MEDICAL CENTER Date: Mar 27, 2026 School of Medicine Esta...Show more

R&D Hardware Test Engineer

Cynet SystemsDurham, NC
Full-time

The R&D Hardware Test Technician is responsible for designing, automating, executing, and supporting verification, validation, and reliability testing activities.This role partners closely with eng...Show more

Sr. Statistical Research Scientist

RhoDurham, North Carolina, US
Full-time

Join us in redefining what it means to work for a CRO.Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to ...Show more

Epidemiological Programmer, Real World Evidence - FSP (Sponsor – Dedicated)

IQVIADurham, North Carolina, US
Full-time +1

IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company.This Epidemiological Programmer role sits within our R...Show more

Principal Statistician.

PSIDurham, NC, US
Full-time +1

You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of bios...Show more

Non-Clinical CMC Statistician, FSP

IQVIADurham, North Carolina, US
Full-time +1

Non-Clinical CMC Statistician, FSP.Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP...Show more

Principal Statistical Programmer

Katalyst HealthCares & Life SciencesDurham, NC
Full-time

Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.Be responsible for overall project delivery, including clinical trial reports and other regulator...Show more

FSP Principal Biostatistician- Early Phase Clinical Development(PK)

IQVIADurham, North Carolina, US
Full-time +1

FSP Senior or Principal Biostatistician for Early Phase Clinical Development (PK).Data Sciences Staffing Solutions, DS3, is a unit within IQVIA that provides our sponsors with fully embedded resour...Show more

Principal Statistical Programmer

IQVIADurham, North Carolina, US
Full-time +1

Job Title: Principal Statistical Programmer.Principal Statistical Programmer.This role requires deep technical expertise, leadership, and hands‑on delivery, covering.SDTM, ADaM, TLF development, an...Show more

Senior Biostatistician

RhoDurham, North Carolina, US
Full-time +2

Join us in redefining what it means to work for a CRO.Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to ...Show more

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SAS Programmer III

SAS Programmer III

Katalyst HealthCares & Life SciencesDurham, NC
30+ days ago
Job type
  • Full-time
Job description

Responsibilities:
  • Review and ensure accurate and high-quality statistical programming deliverables from CRO.
  • Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and guidance documents.
  • Create and maintain specifications as per SDTM/ADaM standard and study SAP.
  • Define and create ad-hoc reports and listings for clinical teams.
  • Develop, implement and maintain SAS programming standards.
  • Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as necessary.
  • Verifies completeness of relevant study deliverables prior to release from the group Maintains all required study documentation.
  • Consults and provides input into system validation efforts including tool maintenance activities.
  • Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.
  • Work in tandem with Biostatistics and Data Management member on various clinical projects.
  • Review CRF annotations and data specifications.
  • Perform quality control on final reports.
  • Develop SAS coding and table templates for preparing, processing and analyzing clinical data.
  • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
  • Perform clinical study report and/or exploratory analysis for oncology clinical study
  • Perform validation of ADaM datasets and TLFs per SAP.
  • Effectively review and comment on vendor programming deliverables and help resolve technical difficulties.
Requirements:
  • BS or above in computer science/statistics with at least years of SAS experience in major pharma or CRO.
  • Develop SAS coding for generating SDTM, ADaM datasets and TLFs to support clinical study analysis
  • Proficient computer skills across multiple applications and OS environments