Refer a freelancer, and you both get 1 free week of DFH Premium. They must use your code {code} at sign-up. More referrals = more free weeks! T&Cs apply.
1 of 5 free roles viewed today. Upgrade to premium for unlimited.

Senior Statistical Programmer

This role is for a Senior Statistical Programmer with a contract length of "unknown", offering a pay rate of "unknown". Requires a BS/BA, 5+ years in statistical programming, SAS proficiency, and oncology experience preferred. CDISC knowledge is essential.
🌎 - Country
United States
💱 - Currency
Unknown
💰 - Day rate
Unknown
Unknown
🗓️ - Date discovered
February 20, 2025
🕒 - Project duration
Unknown
🏝️ - Location type
Unknown
📄 - Contract type
Unknown
🔒 - Security clearance
Unknown
📍 - Location detailed
Dallas, TX
🧠 - Skills detailed
#Macros #Datasets #SAS #Data Review #Data Reconciliation #Documentation #CDISC (Clinical Data Interchange Standards Consortium) #Base #Programming
Role description
You've reached your limit of 5 free role views today. Upgrade to premium for unlimited access.

Responsibilities:

Programs SAS Non-System Edit Checks, Protocol Deviations and SAS Data Listings.
Ability to independently develop innovative and complex SAS programs to support activities including, but not limited to, data review and reporting, and development of patient profiles.
Supports the maintenance of the Non-System Edit Check Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library.
Create SAS program Specifications for Non-System Edit Checks based on CRF and non-CRF data.
Responsible for participating in the development and review of data transfer specifications, processing of clinical data downloads, and data transfers to/from service providers.
Create Clinical Data Review Tools [i.e., Data Listing Reports (DLRs); External Data Reconciliation Listings, Medical Safety Listings for reconciliation, etc.] for all studies based on study-specific specs and requirements.
May oversee development of datasets (SDTMs/ADaMs) in CDISC-compliant format by CROs including clear documentation of the process that was followed in the form of specifications, trackers, and checklists.
May be involved in QC of CRO deliverables like ADaMs, and tables, listings and figures.
Independently develop SAS or other programs and specifications for the production of output to support study needs including publications, safety reporting, and ad hoc analyses in a timely fashion.
Independently verify other programmers' results.
Develop and/or validate standard macros to automate output production.
Adhere to company SOPs and department guidelines.
Work concurrently on multiple projects.
Troubleshoot technical and project issues.
Help with infrastructure development of the department.
Communicate effectively with internal cross-functional groups and external partners.
Requirements:

BS/BA degree in related discipline
At least 5 years of experience in statistical programming with clinical data and SAS.
Experience in oncology therapeutic area strongly preferred.
Strong SAS programming skills required with proficiency in SAS/Base, SAS/Stat and SAS/Macros.
CDISC proficiency required.
SAS/GRAPH experience desirable.
Knowledge of appropriate regulations, industry standards and guidance documents.
Uses broad expertise or unique knowledge and skills to contribute to development of company objectives and principles, and to achieve goals in creative and effective ways.
Good interpersonal communication skills to collaborate effectively with internal cross-functional groups and external partners.