-Designs and develops statistical programs for the assigned project;
-Performs quality control in support of clinical R&D analysis and reporting
-Assists in the review and input into project requirements;
-Maintains documentation as appropriate;
-Completes programming tasks of medium to high complexity;
-Critically reviews requirements and data, identifies gapssuggests solutions and applies expertise on clinical R&D statistical programming activities
-Mentors, trains junior programmers.
-This role requires an in-depth knowledge of SAS programming;
-This role requires a working knowledge of departmental processes, clinical R&D concepts and applicable health authority regulations.
-Bachelor’s degree or higher in computer science, mathematics, health statistics or other scientific field (or equivalent theoretical/technical depth) is required;
-Minimum of 6 years (for bachelor)/3 years (for master) SAS programming experience with increasing responsibility, preferably in a pharmaceutical/clinical trial environment, is required;
-Experience in a pharmaceutical/clinical trial environment is preferred;
-Demonstrated written and verbal communications skill is required;
-Experience working with programmers in a team environment is preferred.Minimum Technical Knowledge and Skills.
Minimum Technical Knowledge and Skills
-Expert knowledge of SAS programming. Knowledge of other statistical software (e.g., S-Plus, R, PASS) is preferred;
-Good communication skills in written and oral English.
J&J (China) Investments Ltd A- Beijing Branch (7075)