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Cdisc Jobs in Florida (NOW HIRING)

YO AI Labs

Biostatistician Expert - Remote

Miami, FL · Remote

$60 - $70/hr

CDISC SDTM & ADaM * SAP interpretation * Survival analysis, mixed models, covariate adjustment * Multiplicity control & ICH E9(R1) * Clinical trial data analysis * TFL production & QC * Regulatory ...

micro1 AI

Director of Biostatistics

Orlando, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Pompano Beach, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Palm Coast, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Tallahassee, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Miami Gardens, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Coral Springs, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Port Saint Lucie, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Miami, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Hollywood, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Pembroke Pines, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Fort Myers, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Fort Lauderdale, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Jacksonville, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

West Palm Beach, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Sunrise, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Tampa, FL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

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$63.1K

$110.1K

$186.1K

How much do cdisc jobs pay per year?

As of Aug 15, 2026, the average yearly pay for cdisc in Florida is $110,070.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,400.00 and $119,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the CDISC position, and why are they important?

To thrive as a CDISC specialist, you need expertise in clinical data standards, data management, and a strong background in life sciences or clinical research. Familiarity with CDISC standards like SDTM, ADaM, and tools such as SAS, Medidata, or clinical data management systems is essential, and certifications in CDISC or related areas are highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills for collaborating with cross-functional teams. These competencies ensure accurate data standardization and compliance in clinical trials, facilitating regulatory submissions and high-quality research outcomes.

What are some common challenges faced by CDISC specialists in clinical research?

CDISC specialists often face challenges such as keeping up with evolving data standards, ensuring data consistency across multiple studies, and coordinating with global teams to align on standard implementation. It is common to manage large, complex datasets while working under tight deadlines to meet regulatory submission timelines. Successfully overcoming these challenges requires strong technical acumen, effective communication with clinical and statistical teams, and proactive problem-solving. If you enjoy collaborating in a dynamic environment and have a passion for data quality and compliance, this role can offer significant professional growth opportunities.

What is a CDISC?

A CDISC job typically involves working with clinical data following CDISC (Clinical Data Interchange Standards Consortium) standards, which ensure consistency and compliance in regulatory submissions. Professionals in CDISC roles manage datasets in formats like SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) to facilitate data analysis and reporting. These roles are common in pharmaceutical, biotech, and clinical research organizations, often requiring expertise in programming languages like SAS and knowledge of FDA submission guidelines.

What are the most commonly searched types of Cdisc jobs in Florida?

The most popular types of Cdisc jobs in Florida are:

What are popular job titles related to Cdisc jobs in Florida?

For Cdisc jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Cdisc jobs in Florida look for?

The top searched job categories for Cdisc jobs in Florida are:

Cdisc jobs near you
Infographic showing various Cdisc job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $110,070 per year, or $52.9 per hour.

Statistical Programmer II

Ruri Software Technologies LLC

Tampa, FL • On-site

Full-time

Re-posted 27 days ago

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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