Clinical Statistical Programmer

This position supports Clinical Data Management activities.

Candidate will works with Statistical Programmer, Biostatistician and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting.

Ensure completeness, correctness and consistency of clinical data and
data structure. Ensures secure and high integrity data transfers from
vendors. Provides timely support to the study team on all routine
programming matters according to the project plan and programming
specification using internal standards and guidelines providing input to CRF/eCRF and programming edits checks. Contributes to the reporting of routine clinical data through regulatory approval, product launch and annual reports. Contributes to the monitoring of data quality during study conduct; providing information on issues along with proposed solutions.
REQUIREMENTS
Knowledge
Excellent verbal and written communication skills and interpersonal
skills are required. General knowledge of pharmaceutical clinical
development and ability to provide routine programming supports needs