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)
 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.