SDTM/Clinical SAS- Visa Independent

Roselle, NJ, US • Posted 1 day ago • Updated 1 day ago
Contract Corp To Corp
Contract Independent
Contract W2
12 Months
No Travel Required
On-site
Depends on Experience
Fitment

Dice Job Match Score™

🎯 Assessing qualifications...

Job Details

Skills

  • SDTM
  • CLINICAL SAS

Summary

1.Must have 6-8 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
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91098872
  • Position Id: 5552-10115-
  • Posted 1 day ago
Contact the job poster
PA

Pooja Agarwal

Recruiter @ Shrive Technologies LLC
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