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Statistical Programmer

Denver, CO · On-site +1

Program SDTM, ADaM, and TLFs, and write detailed dataset specifications. Perform quality control on ... Contract For' seven times by Staffing Industry Analysts as well as a 'Best Company to Work For' by ...

CICONIX, LLC

Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ... TBD . *This position is contingent and will begin upon contract award. CICONIX LLC is an Equal ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ... TBD . *This position is contingent and will begin upon contract award. CICONIX LLC is an Equal ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ... TBD . *This position is contingent and will begin upon contract award. CICONIX LLC is an Equal ...

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior ... Plan, SDTM/ADaM Specification documents, Define packages. Program and validate CDISC compliant ...

Xencor

CON-Statistical Programmer

San Diego, CA · On-site

$75 - $100/hr

The Contract Statistical Programmer supports statistical analysis and reporting for clinical ... Knowledge of CDASH and CDISC standards, including SDTM and ADaM, and experience transforming raw ...

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How much do contract sdtm programmer jobs pay per hour?

As of May 30, 2026, the average hourly pay for contract sdtm programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What is the difference between Contract Sdtm Programmer vs Clinical Data Coordinator?

AspectContract Sdtm ProgrammerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in SDTM and programming languages like SASUsually requires a degree in health sciences, nursing, or related fields, with knowledge of data management
Work EnvironmentContract-based, often remote or on-site at pharmaceutical or CRO companiesFull-time, on-site or remote, working within clinical trial teams
Industry UsageCommonly used in clinical research, pharmaceutical, and CRO settingsUsed in clinical research organizations, hospitals, and pharmaceutical companies

The Contract Sdtm Programmer focuses on programming and data standards for clinical trial data, while the Clinical Data Coordinator manages data collection, entry, and quality. Both roles are essential in clinical research but differ in technical focus and responsibilities.

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Contract Sdtm Programmer jobs near you
Infographic showing various Contract Sdtm Programmer job openings in the United States as of May 2026, with employment types broken down into 5% Full Time, and 95% Contract. Highlights an 100% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.
Clinical SAS Programmer

Clinical SAS Programmer

Katalyst Healthcares & Life Sciences

Newark, NJ

Contractor

Posted 9 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
  • Provides input in the design and development of case report forms and clinical databases.
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
  • Programs for quality checks for clinical study raw data and report the findings to Data Management.
  • Provides input in the design and development of case report forms and clinical study databases.
  • Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.

Requirements:

  • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
  • Ability to prioritize and multi-task effectively.
  • Demonstrated positive attitude and the ability to work well with others.
Additional Information

All your information will be kept confidential according to EEO guidelines.

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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