Proficiency in SAS.
Knowledge of the programming and reporting process.
Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
Demonstrate ability to learn new systems and function in an evolving technical environment.
Strong leadership ability.
Attention to detail.
Ability to successfully work together with a (“virtual”) team (including international teams as required) as well as independently.
Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.
Business/Operational skills that include customer focus, commitment to quality management and problem solving.
Good business awareness/business development skills (including financial awareness).
Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
Work effectively in a quality-focused environment.
Demonstrate commitment to refine quality processes.
Effective time management in order to meet daily metrics or team objectives.
Shows commitment to and performs consistently high quality work.