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Programmer analyst • durham nc

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SAS Programmer III

Katalyst HealthCares & Life SciencesDurham, NC
[job_card.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...[internal_linking.show_more]

Senior Senior Analyst

Piper CompaniesDurham, North Carolina
[job_card.full_time]

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Principal Statistical Programmer, R Programming

IQVIADurham, North Carolina, US
[job_card.full_time] +1

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Compensation Analyst

AA2ITDurham, NC, United States
[job_card.full_time]

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Sr Financial Analyst

BioventusDurham, NC, United States
[job_card.full_time]

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Data Analyst

MillenniumSoftResearch Triangle Park, NC
[job_card.full_time]

Eligibilities & qualifications.[internal_linking.show_more]

Management & Program Analyst

US Government JobsDurham, NC, United States
[job_card.full_time]

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Senior Business Analyst

Fidelity InvestmentsDurham, NC, US
[job_card.full_time]

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

IQVIADurham, North Carolina, US
[job_card.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...[internal_linking.show_more]

Financial Analyst

KBI BiopharmaDurham, NC, United States
[job_card.full_time]

The Financial Analyst must possess a deep understanding of USGAAP with exceptional data analytical skills.The candidate will leverage their accounting expertise and analytical abilities to conduct ...[internal_linking.show_more]

Financial Analyst 8101

Joseph Michaels InternationalDurham, NC
[job_card.full_time]

This is a contract job opportunity.Position: Financial Analyst Location: Durham NC -Remote, but looking for local.Schedule: 8 am -5 pm , M-FProjected duration: 6 months + potential for permJob code...[internal_linking.show_more]

Principal Statistical Programmer

Katalyst HealthCares & Life SciencesDurham, NC
[job_card.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...[internal_linking.show_more]

Business Analyst

IT ExcelDurham, NC, United States
[job_card.full_time]

Evaluating business processes, anticipating requirements, uncovering areas for improvement, and developing and implementing solutions.Leading ongoing reviews of business processes and developing op...[internal_linking.show_more]

QC Analyst I

IntelliPro Group Inc.Durham, NC, US
[job_card.full_time]
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QC Analyst I Duration: 06 months with possible extension Office: Durham, NC, 27709 Pay rate: $30.W2 Position Summary The QC Analyst I, reporting to the Manager of Quality Control, will be responsib...[internal_linking.show_more]

Quality Control Analyst

LancesoftResearch Triangle Park, NC, US
[job_card.full_time]
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The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various departments (incl...[internal_linking.show_more]

Principal Statistical Programmer

IQVIADurham, North Carolina, US
[job_card.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...[internal_linking.show_more]

Project Analyst

ZoetisDurham, NC, United States
[job_card.full_time]

Provides project management support and coordination to multiple research and development teams to ensure execution of operational objectives.This role in partnership with the Project Manager will ...[internal_linking.show_more]

Business Analyst

Omni InclusiveDurham, NC, United States
[job_card.full_time]

Mandatory Skills - Business Analyst With Clinical Regulatory Background.Minimum 5 years of experience in Pharmaceutical/Biotech industry SaaS vendors; relationship with internal business groups.Too...[internal_linking.show_more]

Business Analyst

Tech DigitalDurham, NC, United States
[job_card.full_time]

Mandatory Skills - Business Analyst With Clinical Regulatory Background.Minimum 5 years of experience in Pharmaceutical/Biotech industry SaaS vendors; relationship with internal business groups.Too...[internal_linking.show_more]

SAS Programmer III

SAS Programmer III

Katalyst HealthCares & Life SciencesDurham, NC
[job_card.30_days_ago]
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  • [job_card.full_time]
[job_card.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