The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Up-versioning activities to specific versions of SDTM * Participation in industry teams and ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Up-versioning activities to specific versions of SDTM * Participation in industry teams and ...
The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer ... Critical client project activities are reporting database development (SDTM and ADaM), statistical ...
The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer ... Critical client project activities are reporting database development (SDTM and ADaM), statistical ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Up-versioning activities to specific versions of SDTM * Participation in industry teams and ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Up-versioning activities to specific versions of SDTM * Participation in industry teams and ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Up-versioning activities to specific versions of SDTM * Participation in industry teams and ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Up-versioning activities to specific versions of SDTM * Participation in industry teams and ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be responsible ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be responsible ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be responsible ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be responsible ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Sr SAS Programmer Analyst - SDTM * Responsible for SDTM data creation and delivery for oncology studies. * Prepare ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Sr SAS Programmer Analyst - SDTM * Responsible for SDTM data creation and delivery for oncology studies. * Prepare ...
Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ... Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory ...
Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ... Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory ...
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ... Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory ...
Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ... Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory ...
Manager, Clinical Programming (Remote)
Fairfield, CT · On-site +1
... Senior Clinical Programmer to support clinical development programs by delivering high-quality ... The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern ...
Quick apply
Manager, Clinical Programming (Remote)
Fairfield, CT · On-site +1
... Senior Clinical Programmer to support clinical development programs by delivering high-quality ... The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Manager, Clinical Programming (Remote)
Fairfield, CT · On-site +1
... Senior Clinical Programmer to support clinical development programs by delivering high-quality ... The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern ...
Manager, Clinical Programming (Remote)
Fairfield, CT · On-site +1
... Senior Clinical Programmer to support clinical development programs by delivering high-quality ... The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern ...
The Senior Statistical Programmer will serve as a senior technical expert responsible for end-to ... Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines. * Oversee ...
The Senior Statistical Programmer will serve as a senior technical expert responsible for end-to ... Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines. * Oversee ...
We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and ... Champion industry standards and quality, applying CDISC conventions (CDASH, SDTM, TAUGs ...
We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and ... Champion industry standards and quality, applying CDISC conventions (CDASH, SDTM, TAUGs ...
Senior Manager, Statistical Programming - Job ID: 1646
Palo Alto, CA · On-site
$180K/yr
This position requires expertise in CDISC standards (SDTM, ADaM), strong communication and ... Proven experience as a lead programmer for clinical trials and complex technical projects.
Senior Manager, Statistical Programming - Job ID: 1646
Palo Alto, CA · On-site
$180K/yr
This position requires expertise in CDISC standards (SDTM, ADaM), strong communication and ... Proven experience as a lead programmer for clinical trials and complex technical projects.
This role will serve as lead programmer on assigned clinical trials, working closely with ... Develop, validate, and execute SAS programs and macros to generate SDTM and ADaM datasets and ...
This role will serve as lead programmer on assigned clinical trials, working closely with ... Develop, validate, and execute SAS programs and macros to generate SDTM and ADaM datasets and ...
Senior Manager, Statistical Programming - Job ID: 1646
Palo Alto, CA · On-site
$180K/yr
This position requires expertise in CDISC standards (SDTM, ADaM), strong communication and ... Proven experience as a lead programmer for clinical trials and complex technical projects.
Quick apply
Senior Manager, Statistical Programming - Job ID: 1646
Palo Alto, CA · On-site
$180K/yr
This position requires expertise in CDISC standards (SDTM, ADaM), strong communication and ... Proven experience as a lead programmer for clinical trials and complex technical projects.
Senior Manager, Statistical Programming - Job ID: 1646
Palo Alto, CA · On-site +1
$180K/yr
This position requires expertise in CDISC standards (SDTM, ADaM), strong communication and ... Proven experience as a lead programmer for clinical trials and complex technical projects.
Senior Manager, Statistical Programming - Job ID: 1646
Palo Alto, CA · On-site +1
$180K/yr
This position requires expertise in CDISC standards (SDTM, ADaM), strong communication and ... Proven experience as a lead programmer for clinical trials and complex technical projects.
This role will serve as lead programmer on assigned clinical trials, working closely with ... Develop, validate, and execute SAS programs and macros to generate SDTM and ADaM datasets and ...
This role will serve as lead programmer on assigned clinical trials, working closely with ... Develop, validate, and execute SAS programs and macros to generate SDTM and ADaM datasets and ...
Senior Sdtm Programmer information
See salary details
$13.46 - $18.77
1% of jobs
$18.77 - $24.08
2% of jobs
$24.08 - $29.39
3% of jobs
$29.39 - $34.70
8% of jobs
$34.70 - $40.01
6% of jobs
$43.55 is the 25th percentile. Wages below this are outliers.
$40.01 - $45.32
6% of jobs
$45.32 - $50.63
14% of jobs
The median wage is $53.62 / hr.
$50.63 - $55.94
17% of jobs
$60.96 is the 75th percentile. Wages above this are outliers.
$55.94 - $61.25
19% of jobs
$61.25 - $66.56
13% of jobs
$66.56 - $71.88
11% of jobs
$13
$52
$71
How much do senior sdtm programmer jobs pay per hour?
What is the difference between Senior Sdtm Programmer vs Clinical Data Coordinator?
| Aspect | Senior Sdtm Programmer | Clinical Data Coordinator |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or related field, with experience in SDTM programming | Usually holds a degree in health sciences, nursing, or related field, with data management training |
| Work Environment | Works primarily in clinical trial data programming, using SAS or similar tools | Manages data entry, cleaning, and validation in clinical trial settings |
| Industry Usage | Commonly employed in pharmaceutical and biotech companies for SDTM data standardization | Found in clinical research organizations, hospitals, and pharmaceutical companies |
The main difference is that Senior Sdtm Programmers focus on programming and data standardization using SDTM standards, while Clinical Data Coordinators handle data collection, entry, and quality control. Both roles are essential in clinical trials but differ in technical scope and responsibilities.
What are the typical collaboration points between a Senior SDTM Programmer and clinical data management teams?
What are Senior SDTM Programmers?
What are the key skills and qualifications needed to thrive as a Senior SDTM Programmer, and why are they important?

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 8 days ago
Job description
Job Description
In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards planning activities, coaching and consulting with project teams, outreach to external vendors and partners, and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.
The incumbent will be responsible for continuous improvement of our electronic submission process and providing tools and templates to support delivery focusing on traceability, quality assurance, data conformance and data fitness. The position is a key collaborator with statistical programming, statistics, regulatory and other project stakeholders.
Primary Activities
PreNDA and PreBLA meeting preparation, study data standards plan, preparing questions for FDA e-data mailboxes (CBER/CDER), attendance at meetings with regulatory agencies (FDA, EMA, PMDA),
Guiding project teams preparing submission deliverables including use of Pinnacle 21 Enterprise,
Up-versioning activities to specific versions of SDTM
Participation in industry teams and conferences on best practices
Membership on departmental strategic initiative project teams
Education and Minimum Requirement
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 3 years of SAS programming experience in a clinical trial environment
OR
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years of SAS programming experience in a clinical trial environment
Department Required Skills and Experience
Effective interpersonal skills and ability to negotiate and collaborate effectively
Effective written, oral, and presentation skills
Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders
Position Specific Required Skills and Experience:
US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables
Experience with submission standards CDISC (SDTM, ADaM), Define.XML, SDRG, ADRG
Demonstrated success in the assurance of deliverable quality and process compliance.
Excels in technical writing, able to convert complex ideas and information into simple readable form
Solid project management skills
Familiarity with clinical data management concepts
Strategic thinking - ability to turn strategy into tactical activities
Ability to anticipate stakeholder requirements
Preferred Skills and Experience
Working knowledge or R and Python programming languages for data analysis, automation, and clinical data standards activities
Strong working knowledge of reporting processes (SOPs) and software development life cycle (SDLC)
Experience assuring consistency across protocols and projects
Ability and interest to work across cultures and geographies
Ability to complete statistical programming deliverables through the use of global outsource partner programming staff
Experience developing and managing a project plan using Microsoft Project or similar package
Active in professional societies
Experience in process improvement
eligibleforERP
SPjobs
BARDS2020
VETJOBS
EBRG
Required Skills:
Clinical Trials, Data Management, Data Modeling, Electronic Submissions, Project Management, Stakeholder Relationship Management, Statistical Analysis Systems (SAS) Programming, Study Data Tabulation Model (SDTM)Preferred Skills:
Python (Programming Language), R ProgrammingCurrent Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
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The salary range for this role is
$117,000.00 - $184,200.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
DomesticVISA Sponsorship:
YesTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
07/28/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.