Job Description :
Role : SAS Clinical/Pharma consultant
Location - South San Francisco, CA
Project - CVD (Cardio Vascular Disease) therapeutic study ready for submission
Experience - minimum 5 years Experience with SAS or SQL programming techniques with clinical data management application

SAS for Clinical trials/Pharmaceutical area
o SAS certification preferred
Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and recommended CDM Best Practices.
Logical thinking, attention to detail and accuracy, good organizational skills, and problem-solving abilities.
Ability to thrive in a fast-paced environment
Strong interpersonal and communication (written and verbal) skills.

Looking forward for your response.