
Prudent Technologies and Consulting
North Wales, Pennsylvania • Today
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Depends on Experience
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Prudent Technologies and Consulting
North Wales, Pennsylvania • Today
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Contract
Depends on Experience






Partner's Consulting, Inc.
Hybrid in Philadelphia, Pennsylvania • Yesterday
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Gainwell Technologies LLC
Philadelphia, Pennsylvania • Today
Full-time
USD 86,800.00 - 124,000.00 per year


Lockheed Martin Corporation
Moorestown, New Jersey • Today
Full-time
USD 110,500.00 - 198,422.00 per year



Role: Business Analysis
Location: North Wales, PA
Duration: 6+ Months
Mandatory Skills SDTM, Clinical SAS
Job Description:
Looking for SDTM experts having in-depth knowledge of SAS programming(macro’s)
1.Must have 10+ yrs of exp in clinical domain
2.Strong knowledge of SDTM
3.Create advanced SAS macros, templates, and utilities for efficient data processing
4.Act as the primary programming point of contact for biostatisticians and study teams
5.Perform peer review of code and documentation for accuracy and traceability
6.Review CRF (Case Report Form) annotations and data specifications.
7.Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines
Skill:
1.Extensive programming experience in a clinical trial environment (CRO/Pharma).
2.Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
3.In-depth knowledge of CDISC standards and regulatory submission requirements
👾 Reticulating splines...
Pennsylvania
•
Today
HMG America LLC is the best Business Solutions focused Information Technology Company with IT consulting and services, software and web development, staff augmentation and other professional services. One of our direct clients is looking for SAS Clinical Consultant in Upper Gwynedd, PA. Below is the detailed job description. Title: SAS Clinical Consultant Location: Upper Gwynedd, PA Duration: 6 + Months Primary Skills: SDTM, Clinical SAS Job Description: Looking for SDTM experts having in
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Contract, Third Party
$DOE
Pennsylvania
•
Today
Looking for SDTM experts having in-depth knowledge of SASprogramming(macros) 1.Must have 10+yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS macros, templates, and utilities for efficient data processing 4.Act as the primary programming point of contact for biostatisticians and study teams 5.Perform peer review of code and documentation for accuracy and traceability 6.Review CRF (Case Report Form) annotations and data specifications. 7.Ensure compliance with
Easy Apply
Contract, Third Party
Depends on Experience
Hybrid in North Wales, Pennsylvania
•
Today
Senior Clinical SAS Developer Upper Gwynedd, PA (Onsite) Long Term Contract Employment Type W2 Looking for SDTM experts having in-depth knowledge of SAS programming(macro's) Must have 10+ yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point of contact for biostatisticians and study teams Perform peer review of code and documentation for accuracy and traceability Review CRF (C
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Contract, Third Party
King of Prussia, Pennsylvania
•
Today
The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas. The individual will work closely with the Senior Director, Clinical and
Full-time
Compensation information provided in the description