Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports ...
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports ...
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports ...
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports ...
Biostatistician Expert - Remote
Dallas, TX · 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 ...
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Biostatistician Expert - Remote
Dallas, TX · 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 ...
Biostatistician Expert - Remote
Austin, TX · 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 ...
Quick apply
Biostatistician Expert - Remote
Austin, TX · 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 ...
Biostatistician Expert - Remote
Houston, TX · 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 ...
Quick apply
Biostatistician Expert - Remote
Houston, TX · 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 ...
Regulatory Data Manager
Plano, TX · Remote
Ensure compliance with: o FDA regulations o 21 CFR Part 11 o CDISC standards o HIPAA o ICH-GCP o GDPR (where applicable) o Internal SOPs and quality requirements, including documentation of data ...
Regulatory Data Manager
Plano, TX · Remote
Ensure compliance with: o FDA regulations o 21 CFR Part 11 o CDISC standards o HIPAA o ICH-GCP o GDPR (where applicable) o Internal SOPs and quality requirements, including documentation of data ...
Statistical Programmer II
Austin, TX · On-site
$90K - $100K/yr
Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...
Statistical Programmer II
Austin, TX · On-site
$90K - $100K/yr
Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...
Regulatory Data Manager
Plano, TX · On-site +1
... CDISC standards o HIPAA o ICH-GCP o GDPR (where applicable) o Internal SOPs and quality requirements, including documentation of data accuracy, integrity, security, audit trails, and regulatory ...
Regulatory Data Manager
Plano, TX · On-site +1
... CDISC standards o HIPAA o ICH-GCP o GDPR (where applicable) o Internal SOPs and quality requirements, including documentation of data accuracy, integrity, security, audit trails, and regulatory ...
Statistical Programmer II
Dallas, TX · On-site
$90K - $100K/yr
Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...
Statistical Programmer II
Dallas, TX · On-site
$90K - $100K/yr
Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...
Statistical Programmer II
Houston, TX · On-site
$90K - $100K/yr
Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...
Statistical Programmer II
Houston, TX · On-site
$90K - $100K/yr
Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...
Director, Clinical Data & AI
Austin, TX · On-site +1
Drive standardization (e.g., CDISC-based models) and elimination of data silos 3. AI, Data Science & Advanced Analytics * Lead development and deployment of AI/ML capabilities across the clinical ...
Director, Clinical Data & AI
Austin, TX · On-site +1
Drive standardization (e.g., CDISC-based models) and elimination of data silos 3. AI, Data Science & Advanced Analytics * Lead development and deployment of AI/ML capabilities across the clinical ...
Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas. * Understand the various tools that we work with * High level ...
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Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas. * Understand the various tools that we work with * High level ...
Director, Clinical Data & AI
Fort Worth, TX · On-site +1
Drive standardization (e.g., CDISC-based models) and elimination of data silos 3. AI, Data Science & Advanced Analytics * Lead development and deployment of AI/ML capabilities across the clinical ...
Director, Clinical Data & AI
Fort Worth, TX · On-site +1
Drive standardization (e.g., CDISC-based models) and elimination of data silos 3. AI, Data Science & Advanced Analytics * Lead development and deployment of AI/ML capabilities across the clinical ...
Cdisc information
See Texas salary details
$78.7K - $92.7K
3% of jobs
$92.7K - $106.6K
10% of jobs
$116K is the 25th percentile. Wages below this are outliers.
$106.6K - $120.5K
18% of jobs
The median wage is $134.5K / yr.
$120.5K - $134.5K
19% of jobs
$146.6K is the 75th percentile. Wages above this are outliers.
$134.5K - $148.4K
29% of jobs
$148.4K - $162.3K
10% of jobs
$162.3K - $176.3K
12% of jobs
$176.3K - $190.2K
0% of jobs
$190.2K - $204.1K
0% of jobs
$204.1K - $218K
0% of jobs
$218K - $232K
0% of jobs
$78.7K
$137.2K
$232K
How much do cdisc jobs pay per year?
As of Sep 1, 2026, the average yearly pay for cdisc in Texas is $137,225.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,500.00 and $149,100.00 per year, depending on experience, location, and employer.
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 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 are the most commonly searched types of Cdisc jobs in Texas?
The most popular types of Cdisc jobs in Texas are:
What are popular job titles related to Cdisc jobs in Texas?
For Cdisc jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Cdisc jobs in Texas look for?
The top searched job categories for Cdisc jobs in Texas are:
Job description
Clinical Data Manager
The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements. This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution.
Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol. Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams. Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations.
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports (CSRs). Serve as the primary point of contact for data management vendors and oversee their deliverables. Participate in study team meetings and provide status updates related to data quality and timelines. Support audit readiness and participate in regulatory inspections when required.
Bachelor's degree in Life Sciences, Computer Science, Health Informatics, or related field. Minimum of 3–5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment. Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong understanding of ICH-GCP, FDA regulations, and CDISC standards. Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug). Excellent organizational, analytical, and problem-solving skills. Strong communication and collaboration skills across cross-functional teams.
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