Dear Business Partner,
My client is looking for a SAS Clinical Programmer.
Please share your consultants suitable resumes with me on my ID:
[email protected];

Job Title:            SAS Clinical Programmer
Location:            Santa Rosa, CA
Duration:            6+ Months Contract

*Write-Up Criteria:*
REQUIRED: SAS programming experience in a clinical trial environment (you
will see this on resumes – reference attached candidate)
REQUIRED: Submit a sample SAS code with each candidate.

**upon offer, candidates must complete background check and drug test**

Responsibilities:
Plans and coordinates programming, testing, and documentation of
statistical programs for use in creating statistical tables, graphics, and
listing summaries.
Programs analysis database manipulations and transfers of data for internal
and external clients.
May integrate databases from multiple studies or sources.
Develops listing and table specifications with study Biostatistician.
Interact with Data Management and Biostatistics staff and SP team members
to negotiate timelines, responsibilities, and deliverables.
Understands and complies with Standard Operating Procedures and Work
Instructions.
Programs, tests, and documents statistical programs and tools in accordance
with SP standards and validation procedures.
Will be working on Endovascular trials; Vascular Biostat and data
management group.

Candidate Requirements:
Experience using SAS for more than 2 years and using SAS on clinical trial
data analysis.
Industrial experience is preferred
Regulatory submission experience is a plus
Prefer the candidate has industry experience and had experience with PMA
submission etc.
Absolute skill is SAS programming skills inlcuding SAS BASE/STAT/MACRO/SQL
etc.

Thank you for your time and look forward to work with you.
______________________________________

Thanks,
David Johnson - Sr IT Recruiter
MANIFEST Technology
Email: [email protected]

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