Statistical Programmer Consultant

Innova Solutions•Austin, TX

3d•Remote

About The Position

Innova Solutions has a client that is immediately hiring for a Statistical Programmer Consultant. This is a Full Time Contract position with a duration of 6 months, located remotely.

Requirements

Statistical programming support for Phase 1 to Phase 3 studies
Project integration and disease monitoring project work
Programming SDTM/ADaM/TLFs
Writing datasets specification
QC datasets and tables
Programming activities on multiple projects/ studies across various therapeutic areas
Creating and reviewing annotated CRF to SDTM datasets
Balancing conflicting priorities
Promoting communication and adequate information flow
Setting high expectations for quality, creativity and project ownership
Collaborating with Clinical Operations, Clinical Data Management, Global Drug Safety, Regulatory and Project Management
Providing technical input into documents produced by other functions
Development and maintenance of data review and reporting tools
Development of any other statistical applications as appropriate
Involvement with strategy for process improvement
Identifying new tools to increase efficiency and quality

Responsibilities

Working with the Biometrics staff, the Statistical Programmer Consultant provides programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work.
Provides timely support to the project team on all statistical programming matters according to the project strategy.
Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables.
Involved in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs
Creates and reviews annotated CRF to SDTM datasets
Provides support in balancing conflicting priorities, promoting communication and adequate information flow to motivate, encourage and align people with the company's strategic objectives
Functions as a positive role model for setting high expectations for quality, creativity and project ownership
Works collaboratively with Clinical Operations, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting
Provides technical input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers)
Works with Biometrics and other functions for the development and maintenance of the data review and reporting tools, and any other statistical applications as appropriate
Involved with the strategy for process improvement
Identifies new tools to increase efficiency and quality