Prepare various reports for all designs and database and analyze same and evaluate all study protocols for all clinical activities.
Coordinate with all medical groups and prepare scientific reports and develop all statistical plans for all clinical programs life cycle.
Provide expertise statistical knowledge and ensure optimization of all clinical trial designs and analyze all statistics and prepare reports for all programs.
Develop all statistical analysis plans according to program standards for all clinical programs and prepare annual study reports and maintain records of all results to be submitted to management.
Collaborate with clinical development team and director of biostatistics and analyze all statistics for all programs and provide training to all juniors for clinical trail designs.
Monitor all external data management functions and monitor efficient work of all internal and external bioanalysts programmers.
Participate in all regulatory meetings for clinical programs and maintain knowledge on all statistical methods and procedures.