- Provide statistical inputs/consultants on trial design, protocol and CRF development, perform sample size calculation, interact with clients with regard to statistical issues
- Authoring and review of statistical analysis plans and statistical methodology sections in clinical protocols in different therapeutic areas from phase I to phase IV
- Manage team activities including training and mentoring, issues resolving, quality control and timely completion of project deliverables, ensure on-time deliver best value and high-quality service
- Develop, review and improve standard operation procedures (SOPs), working instructions (WIs), standard templates and procedures to ensure all activities in accordance with internal and external quality standards, SOPs/WIs, ICH-GCP and/or any other applicable local and international regulations, guidelines and industry standards and improve productivity and efficiency of the team
- Maintain a positive, collaborative, results orientated work environment, build partnerships and teamwork, communicate to team in an open, transparent and objective manner