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Clinical R Programmer Jobs in Florida (NOW HIRING)

Health Network One

Lead Clinical Analyst

Miami, FL · On-site

Position Summary The Lead Clinical Analyst drives enterprise clinical performance strategy by ... Experience with data science tools and programming languages such as Python or R Equal Opportunity ...

Jacobs Management Group

Packaging Engineer

Alachua, FL

$65K - $80K/yr

If you want your engineering work to carry real clinical weight, this is where to do it. Why you ... Comfortable applying process validation methodology (IQ, OQ, PQ) and statistical tools (Gage R&R ...

University of Miami

Asst. Scientist

Miami, FL

... clinical trials, observational studies, and animal studies. Experience with omics data (such as genomics, proteomics, metabolomics), and bioinformatics tools. Proficiency in R programming, with ...

The University of Miami

Asst. Scientist

Miami, FL · On-site

... clinical trials, observational studies, and animal studies. • Experience with omics data (such as genomics, proteomics, metabolomics), and bioinformatics tools. • Proficiency in R programming ...

Moffitt Cancer Center

Research Software Engineer

Tampa, FL · On-site

$193K/yr

... clinical, and imaging datasets. (30%) • Provide documentation and user support enabling ... as R, Perl, C#, and Java. • Experience developing web-based and/or scientific software that ...

The University of Miami

Sr. Software Engineer

Miami, FL · On-site

$117K - $154K/yr

... clinical environments * Master's degree in Computer Science, Software Engineering, or a related field. * Experience with other programming languages, such as Python or R * Experience with other ...

University of Miami

Sr. Software Engineer

Miami, FL

$117K - $154K/yr

... clinical environments * Master's degree in Computer Science, Software Engineering, or a related field. * Experience with other programming languages, such as Python or R * Experience with other ...

TRIMEDX Holdings

Imaging Engineer II

Middleburg, FL

... R/F, portables, C-arms, mammography, Nuclear Medicine, CR, DR, ultrasound, bone density, and all ... Maintain Clinical Engineering expertise through ongoing training and education * Assist with ...

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Clinical R Programmer information

What are the key skills and qualifications needed to thrive as a Clinical R Programmer, and why are they important?

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are Clinical R Programmers?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What are some common challenges faced by Clinical R Programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Florida? For Clinical R Programmer jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Florida look for? The top searched job categories for Clinical R Programmer jobs in Florida are:
What cities in Florida are hiring for Clinical R Programmer jobs? Cities in Florida with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you
Statistical Programmer II

Statistical Programmer II

Ruri Software Technologies LLC

Tampa, FL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Role: Statistical Programmer II
Location : Tampa, Florida
Job Duties:
Roles and responsibilities she perfomed as a Statistical Programmer I/ Sas Programmer I from
Sep2019 - Jan2021 Includes the follows:
Provide statistical programming support for the reporting of clinical trial results of Phase 1
and Phase 2
Experience working with systems used within the Clinical Trial process.
Generated program as per STDM standards and Documentation of SAS code, log, Output
and report as per SOP guidelines.
Performed CDISC Mapping for Ongoing clinical trials and classified data into domains.
understanding with CDISC SDTM Implementation Guide v3.1.2/ v3.1.3 and SDTM
Model.
Proficient in generating clinical reports for safety analysis in the form of tables and listings.
Developed reports for safety as per study requirements debugging SAS errors and
identifying issues producing reports or analysis data sets and SAS data sets.
Roles and responsibilities she perfomed as a Statistical Programmer II/ Sas Programmer II from
feb2021 - Dec2022 Includes the follows:
Experienced in Writing statistical programs using SAS and R as per requests from internal
or external clients and reviewing the statistical analysis plan (SAP), SDRG and ADRG.
Handling of multiple Projects of client data to analyze Phase II and Phase III Clinical trials
data in various therapeutic areas like Hematology, endocrinology, Dermatology,
Gastroenterology, Immunology, Neurology and Virology to provide statistical
programming by using SAS tools such as SAS/MACROS, SAS/SQL and R experience for
the reporting of clinical trial results.
Involved in error handling, fixing bugs, and overcoming the challenges faced while
developing the code of specified structure of Tables and listings through creating Macros
and macro variables.
Experienced in data validation and data cleaning and worked understanding with CDISC
SDTM Implementation Guide v3.2/v3.3 and SDTM Model checks (through specifications) on
clinical trial datasets and QC of Statistical/ Programming outputs like Analysis Datasets and
aCRF (Case Report Form).
Experienced in creating reports using proc report and derived data sets (SDTM, CDISC,
ADAM) and Generated Define.xml output for FDA regulatory submissions.
Created efficacy customize reports for FDA regulatory submissions and develop to
maintain SAS programs to create SDTM and Adam datasets and created Tables and
Figures to support clinical trials.
Track clinical trial milestones for statistical programming deliverables.
Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and
international regulations, and participate in internal/external audits and regulatory
inspections as required.
Analyzed and validated data sets and SAS outputs with other programmer's outputs and
mockups in SAP using PROC COMPARE, PROC CONTENTS and PROC FREQ. Created
formats for the coded data and used PROC SQL for data validation.

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