MS Data Integration
New York, NY · On-site
Expert in addressing technical challenges that connect SAS, CDISC and XML. * Excellent technical skills in SAS system and application development. SDTM. * Proven experience in development and ...
MS Data Integration
New York, NY · On-site
Expert in addressing technical challenges that connect SAS, CDISC and XML. * Excellent technical skills in SAS system and application development. SDTM. * Proven experience in development and ...
SAS Programmer
Falls Church, VA · On-site +1
Develop SAS programs for tables, listings, and figures (TLFs) Create CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data ...
SAS Programmer
Falls Church, VA · On-site +1
Develop SAS programs for tables, listings, and figures (TLFs) Create CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data ...
The Biostatistician will develop FDA-ready, CDISC-compliant deliverables, execute analyses per the approved Statistical Analysis Plan (SAP), and support generation of regulatory-submission outputs ...
The Biostatistician will develop FDA-ready, CDISC-compliant deliverables, execute analyses per the approved Statistical Analysis Plan (SAP), and support generation of regulatory-submission outputs ...
SAS Programmer
Falls Church, VA · On-site
Requirements Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs ...
SAS Programmer
Falls Church, VA · On-site
Requirements Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs ...
MS Data Integration
New York, NY · On-site
Expert in addressing technical challenges that connect SAS, CDISC and XML. * Excellent technical skills in SAS system and application development. SDTM. * Proven experience in development and ...
MS Data Integration
New York, NY · On-site
Expert in addressing technical challenges that connect SAS, CDISC and XML. * Excellent technical skills in SAS system and application development. SDTM. * Proven experience in development and ...
The CDISC Expertise This Role Requires This is worth being precise about, because it defines who fits. What we need: someone who can look at source data and design the system that gets it correctly ...
The CDISC Expertise This Role Requires This is worth being precise about, because it defines who fits. What we need: someone who can look at source data and design the system that gets it correctly ...
Oversee and validate vendor programming activities, including CDISC implementation and analysis reporting * Support creation and validation of e-submission requirements, including annotated CRFs ...
Oversee and validate vendor programming activities, including CDISC implementation and analysis reporting * Support creation and validation of e-submission requirements, including annotated CRFs ...
SAS Programmer
Falls Church, VA · On-site
Create CDISC-compliant datasets (SDTM and ADaM) * Validate and document programming outputs * Collaborate with statisticians and data management teams * Support regulatory submissions and audits ...
Quick apply
SAS Programmer
Falls Church, VA · On-site
Create CDISC-compliant datasets (SDTM and ADaM) * Validate and document programming outputs * Collaborate with statisticians and data management teams * Support regulatory submissions and audits ...
SAS Programmer Lead
North Wales, PA · On-site
In-depth knowledge of CDISC standards and regulatory submission requirements
Quick apply
SAS Programmer Lead
North Wales, PA · On-site
In-depth knowledge of CDISC standards and regulatory submission requirements
Senior Manager, Clinical Data Management
Redwood City, CA · On-site
$170K - $200K/yr
Responsible for accuracy, completeness, and CDISC compliance of Corcept clinical databases. Responsibilities: * Provides input into the design of data flow across EDC and non-EDC data sources across ...
Senior Manager, Clinical Data Management
Redwood City, CA · On-site
$170K - $200K/yr
Responsible for accuracy, completeness, and CDISC compliance of Corcept clinical databases. Responsibilities: * Provides input into the design of data flow across EDC and non-EDC data sources across ...
Statistical Programmer II
Tampa, FL · On-site
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 ...
Statistical Programmer II
Tampa, FL · On-site
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 ...
The individual should have expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML. Excellent technical skills in EDC and SAS systems and application development. Experience ...
The individual should have expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML. Excellent technical skills in EDC and SAS systems and application development. Experience ...
Clinical Database Developer
Fort Detrick, MD · On-site
$125K - $150K/yr
The individual ensures clinical databases meet FDA regulatory requirements, ICH guidelines, Good Clinical Data Management Practices (GCDMP), and CDISC standards, while supporting data collection ...
Quick apply
Clinical Database Developer
Fort Detrick, MD · On-site
$125K - $150K/yr
The individual ensures clinical databases meet FDA regulatory requirements, ICH guidelines, Good Clinical Data Management Practices (GCDMP), and CDISC standards, while supporting data collection ...
Maintain a complete and in-depth understanding of all CDISC guidance documents and implementation guides, as well as FDA guidance and regulation on electronic submission of data; keep abreast of ...
Maintain a complete and in-depth understanding of all CDISC guidance documents and implementation guides, as well as FDA guidance and regulation on electronic submission of data; keep abreast of ...
Clinical SAS Programmer
Chantilly, VA · Remote
Create and validate CDISC-compliant SDTM domains and ADaM datasets using SAS. * Prepare mapping specifications from CRF and other raw data sources to appropriate SDTM domains. * Develop ...
Quick apply
Clinical SAS Programmer
Chantilly, VA · Remote
Create and validate CDISC-compliant SDTM domains and ADaM datasets using SAS. * Prepare mapping specifications from CRF and other raw data sources to appropriate SDTM domains. * Develop ...
The individual ensures clinical databases meet FDA regulatory requirements, ICH guidelines, Good Clinical Data Management Practices (GCDMP), and CDISC standards, while supporting data collection ...
The individual ensures clinical databases meet FDA regulatory requirements, ICH guidelines, Good Clinical Data Management Practices (GCDMP), and CDISC standards, while supporting data collection ...
Design, develop, and validate SDTM and ADaM datasets in compliance with CDISC standards * Lead generation of define.xml, aCRF/eCRF annotations, and submission-ready deliverables * Develop and ...
Quick apply
Design, develop, and validate SDTM and ADaM datasets in compliance with CDISC standards * Lead generation of define.xml, aCRF/eCRF annotations, and submission-ready deliverables * Develop and ...
Active participation in CDISC teams preferred Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law ...
Quick apply
Active participation in CDISC teams preferred Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law ...
Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)
North Chicago, IL · On-site
Active participation in CDISC teams preferred Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)
North Chicago, IL · On-site
Active participation in CDISC teams preferred Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
Associate Director, Clinical Data Management
Redwood City, CA · On-site
$229K - $269K/yr
Responsible for accuracy, completeness and CDISC compliance of Corcept clinical databases. Responsibilities: * Works in cooperation with Director of Clinical Data Management to select and maintain ...
Associate Director, Clinical Data Management
Redwood City, CA · On-site
$229K - $269K/yr
Responsible for accuracy, completeness and CDISC compliance of Corcept clinical databases. Responsibilities: * Works in cooperation with Director of Clinical Data Management to select and maintain ...
Cdisc information
See salary details
$84.5K - $99.5K
3% of jobs
$99.5K - $114.4K
10% of jobs
$124.5K is the 25th percentile. Wages below this are outliers.
$114.4K - $129.4K
18% of jobs
The median wage is $144.3K / yr.
$129.4K - $144.3K
19% of jobs
$157.3K is the 75th percentile. Wages above this are outliers.
$144.3K - $159.3K
29% of jobs
$159.3K - $174.2K
10% of jobs
$174.2K - $189.2K
12% of jobs
$189.2K - $204.1K
0% of jobs
$204.1K - $219.1K
0% of jobs
$219.1K - $234K
0% of jobs
$234K - $249K
0% of jobs
$84.5K
$147.3K
$249K
How much do cdisc jobs pay per year?
As of Sep 14, 2026, the average yearly pay for cdisc in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 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.
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MS Data Integration
New York, NY • On-site
Sonsoft Inc
• IT Services • 51 - 200 employees51 - 200 employees
Full-time
Re-posted 28 days ago
Job description
Company Description
Sonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Software Development, Software Consultancy and Information Technology Enabled Services.
Job Description
Job Description:-
- Expert in addressing technical challenges that connect SAS, CDISC and XML.
- Excellent technical skills in SAS system and application development. SDTM.
- Proven experience in development and implementation of clinical standards in a global pharmaceutical environment.
- Expert in integrating SAS with other leading technologies such as PDF, XML, Microsoft Office, to support electronic submissions.
- Experience in consulting projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle.
- Annotate CRFs in accordance with CDISC published or company specific guidelines with appropriate metadata to reflect case report tabulation data sets.
Primary Skill Microsoft Data Integration Tools
Qualifications
Basic Qualifications :-
- Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
Additional Information
Note:-
This is a Contract job opportunity for you.
Only Only US Citizen, Green Card Holder, H4-EAD, GC-EAD, TN Visa, OPT-EAD & L2-EAD can apply.
No H1B
Please mention your Visa Status in your email or resume.
About Sonsoft
Sourced by ZipRecruiter
Sonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Software Development, Software Consultancy and Information Technology Enabled Services.
Industry
It services
Company size
51 - 200 Employees
Headquarters location
Alpharetta, GA, US
Year founded
2007