As a leading full-service global CRO, we work to create solutions that advance new treatments from discovery to reality.
3355+ employees
B2BHealthcareScienceClinical Trials
Role
Who you are
Must be computer literate and numerate with a willingness to adapt to various computer systems
Hands-on expert level project statistical programmer experienced in providing programming leadership to projects
Statistical programming skills and knowledge across a broad range of applications together with key competencies in customer focus delivering on commitments building strong relationships communicating and influencing and embracing innovation and change
Desirables
SAS/Macro knowledge
Proc Report experience
ODS proficiency
SAS/Graph skills
Proc SQL skills
SAS/STAT skills
What the job involves
Develop test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets tables figures and listings (TFL)
Perform review and provide guidance on the development of the clinical database specification data transfer agreement/specification and specification of tables figures and listings (TFL) shells
Develop and review specification for SDTM datasets and ADaM datasets for safety data TFL shells and other specifications e.g. patient profiles OPS reports
Develop and review electronic data submission package (SDTM annotated CRF define.xml Study/Analysis Data Reviewer's Guide) for high complexity studies
Worldwide Clinical Trials is dedicated to advancing new treatments in partnership with biotechnology and pharmaceutical companies. With a focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, the organization utilizes a collaborative and personalized approach to develop solutions that improve patients' lives through innovative therapies.