Statistical Programmer II

When our values align, there's no limit to what we can achieve.

​Responsibilities :

Act as an internal Subject Matter Expert and Work independently to support various programming activities related to analysis and reporting of clinical study data.

Perform as Statistical Programming Coordinator on projects and interact with Sponsors, Data Operation Lead and other functions as a key contact with regard to statistical programming issue.

Use efficient programming techniques to produce and QC of derived datasets and TLF.

Create / modify standard macros and applications to improve the efficiency.

Develop wider knowledge of SAS and other relevant programming languages and processes.

Understanding regulatory requirements concerning industry technical standards, maintain all supporting documentation in accordance with WSOPs / guidelines.

Provide relevant training and mentorship to staff and project teams A graduate or Master degree in a relevant educational filed life science, computer, pharmacy, others.

Proficiency in SAS and knowledge of programming and reporting process. Excellent experience with TLF, SAS coding, Macros, SQL, PROC reports, SDTM, ADAM(preferred)

Requirements :

Knowledge of WSOPs / ICH-GCP and System Life Cycle methodologies.

Excellent communication (written & oral) skills and strong leadership ability.

Strong organizational skills, flexible to change and team work.

Ability to manage complex projects and business operational skills Study lead experience.

For Associate Manager and Manager Role you must have people management (LM)experience.

First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent

Competent in written English.

Good communication skills.