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clinical sas programmer onsite project

Silicon Staff inc
Woodcliff Lake, New Jersey, United States
April 15, 2019


· Good knowledge of CDISC data structures as well as a solid understanding of the development and use of standard programs

· Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, ICH) and clinical study practices, procedures and methodologies.

· Good communications and negotiation skills, ability to work well with others globally.

· Strong expertise in tables, listings and figure programming is required

· Maintain up-to-date advanced knowledge of programming software (e.g. SAS) as well as CDISC requirements (SDTM, ADaM, eCTD, Define.xml), attend functional meetings and trainings.

Review eCRF, discuss data structures and review activities as member of the Data Review Team.

Comply with company, department and CDISC standards and processes, assess and clarify additional programming requirements at project-level, review and develop programming specifications as part of the analysis plans.

· Ideally 5+ years of work experience in a programming role preferably supporting clinical trials/ or in pharmaceutical industry