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Last updated: 2 days 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

INFORMATION TECHNOLOGY - DUKE TEMPORARY SERVICE

Duke HealthDurham, NC, US
Temporary

INFORMATION TECHNOLOGY - DUKE TEMPORARY SERVICE.Work Arrangement: Requisition Number: 259973 Regular or Temporary: Temporary Location:.Personnel Area: CENTRAL ADMIN MANAGEMENT CTR Date: Apr 1, 2026...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

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

Junior Data Scientist/Analyst/Java full stack developer

Synergistic itResearch Triangle Park, NC, US
Full-time

Struggling to Get Hired by Companies? We can Get you Hired with a plan Many job seekers feel stuck because the tech market has become more competitive, automated, and unpredictable.But your career ...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 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

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

junior java full stack developer/Data scientist

SynergisticITDurham, NC, US
Full-time

Career Gap? Rebuild Momentum and Get Back Into the Market.If you've been unemployed for 3–6+ months—or longer—you've probably seen how quickly the market can change.A career gap can reduce callback...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