Top 91 Sr statistical programmer Jobs

Sr Statistical Programmer
Clinical Data Solution —Massachusetts
- Full-time
- Remote
- 3 years
- Master's degree
- Bachelor's degree
Statistical Programmer/Sr. Statistical Programmer
Arrowhead Pharmaceuticals —Los Angeles, CA
- $90,000 - $135,000 a year
- Master's degree
- Analysis skills
- Quality control
Sr.Statistical Programmer
Katalyst Healthcares & Life Sciences —Boulder, CO
- Contract
- Computer science
- 6 years
- Computer Science
Quick Apply
Sr. Statistical Programmer
Katalyst Healthcares & Life Sciences —Baltimore, MD
- Contract
- Computer science
- 6 years
- Computer Science
Quick Apply
SR. STATISTICAL PROGRAMMER
TruMinds Clinical —Frisco, TX
- $81,286 a year
- Full-time
- Management
- Computer Science
- Mid-level
Sr. Statistical Programmer
SRNL International —Jersey City, NJ
- Computer science
- Computer Science
- 5 years
Senior Statistical Programmer
MM Infotech —Remote
- Full-time
- Remote
- Senior level
Sr. Statistical Programmer
Kodiak Sciences Inc. —Palo Alto, CA
- Full-time
- Computer Science
- 5 years
- Bachelor of Science
Sr Statistical Programmer (NA Only)
Syneos - Clinical and Corporate - Prod —North Carolina
- $80,600 - $145,000 a year
- Full-time
- English
- Team management
- Travel
- Employee stock purchase plan
- Health insurance
Sr Statistical Programmer (NA Only)
サイネオス・ヘルス —Morrisville, NC
- $80,600 - $145,000 a year
- English
- Team management
- Travel
- Employee stock purchase plan
- Health insurance
Senior Statistical Programmer
TEKaroon —Elkridge, MD
- Email
- Computer Science
- Analysis skills
- Mentoring
Senior Statistical Programmer
Navitas Life Sciences —Remote
- Full-time
- Remote
- Computer Science
- Windows
- Master's degree
Sr. Statistical Programmer – Level 1
Clymb Clinical —Burlington, MA
- Full-time
- Computer Science
- Mid-level
- Office
SR. STATISTICAL PROGRAMMER ANALYST
TruMinds Clinical —Frisco, TX
- $81,286 a year
- Full-time
- Mid-level
- Office
- Master's degree
Senior Principal Statistical Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Contract
- 6 years
- Doctor of Philosophy
- Organizational skills
Quick Apply
Senior RWE/RWA Programmer
Parexel —Remote
- Remote
- Writing skills
- English
- Analysis skills
Senior Programmer
SimulStat —Remote
- Contract
- Computer Science
- Master's degree
- SQL
Sr Statistical Programmer (Oncology), Real World Evidence – FSP
IQVIA —Durham, NC
- $88,300 - $220,900 a year
- Full-time
- 3 years
- Master's degree
- SQL
4d
Senior Statistical Programmer
Katalyst Healthcares & Life Sciences —Lake Villa, IL
- Contract
- Computer science
- 6 years
- Computer Science
Quick Apply
Senior Statistical Programmer
Merck —Rahway, NJ
- $117,000 - $184,200 a year
- Full-time
- Computer science
- Computer Science
- Bachelor of Science
- Paid holidays
- Health insurance
10d

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Sr Statistical Programmer

Clinical Data Solution
Massachusetts

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Job Details

Full-time

Qualifications

FDA submissions
Statistics
Database systems
SAS
SAS language
CDISC standards
Quality control operations
Regulatory compliance analysis
Clinical research documentation
Statistical analysis tools
Metadata creation

Full Job Description

Full Time

REMOTE, MA 1 Year Ago

Job Description

Responsibilities:

Conduct a comprehensive review of study documents, including Protocol, CRF, and SAP.
Create and assess statistical programs in SAS and/or R to produce CDISC-compliant SDTM and ADaM datasets.
Execution of validation and quality control procedures for programs, datasets, and statistical reports, ensuring alignment with study requirements.
Development and review CDISC SDTM and ADaM mapping specifications.
Produce and review Tables, Figures, and Listings (TFLs) in accordance with the SAP.
Review datasets for any pending compliance issues and meticulously document identified issues.
Generation and review of submission documents like define.xml, SDTM annotated CRF, and reviewers guide.
Generation of utility macros and efficient code writing to streamline programming processes.
Communicate effectively within project teams to ensure the timely and budget-compliant completion of assigned tasks.
Adherence to Clymb and/or client’s Policies and Procedures.

Requirements:

Master’s degree or equivalent, along with relevant formal academic/vocational qualifications and a minimum of 5 years of SAS programming experience. Alternatively, a Bachelor’s degree with 7+ years of SAS programming experience.
A minimum of 3 years of hands-on CDISC implementation experience. Any experience with R programming will be considered a significant plus.
Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.
Previous involvement as a production or QC programmer at both product and study levels.
Strong organizational, interpersonal, leadership, and communication skills.
Ability to autonomously manage multiple tasks and projects.
In-depth understanding of FDA regulatory guidance around Study Data and Submission, including familiarity with the Study Data Technical Conformance Guide, FDA Data Submission Standards Catalog, and associated requirements.
A minimum requirement of a strong understanding of CDISC Metadata Submission Guidelines (MSG), Define standards, CDASH, SDTM, ADaM, and controlled terminology standards.

Skills:

Statistical Programming

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