Clinical SAS Developer

Role: Clinical SAS Developer Location: Upper Gwynedd, PA /Rahway, NJ Job description: 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 wi

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 progr

Job Description: Design, build, and configure clinical study databases in EDC/CDM platforms. Ensure systems meet client needs, follow GCDMP, support accurate data capture, workflows, edit checks, and integrations. Responsibilities: Lead Study Build / Database Configuration in EDC systems. Configure Edit Checks, Workflows, Validations. Gather & translate client requirements into solutions. Create Specifications / Test Cases / UAT Support. Support integrations & data transfers with vendors. Deliv

Job Description COA Sr. Specialist is responsible for providing end-to-end COA systems project management support including, but not limited to, gathering study-specific user requirements, executing UAT tasks, managing project timelines, managing and enforcing COA systems Standards. COA Sr. Specialist also monitors system change requests and acts as our Company's COA systems subject matter expert while liaising with external vendors. Accountable for making decisions regarding COA process, issue