• 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.