**General Description:** Manager leads patient-centric projects, PRO publications and provide trainings to internal cross functional teams. Supports the design, delivery, and execution of clinical outcomes assessment (COA) strategies. Manager will coordinate team meetings and will collaborate with the cross functional teams, review and author PRO sections of clinical documents, i.e., protocols, SAPs, CSRs, SCEs, coauthor publications and will develop presentations. The Manager will stay informed of the latest regulatory and HTA requirements and will take part in regulatory submission and response documents. The Global manager will assist with the psychometric methods of the post hoc analyses of the PRO data from clinical trials. **Essential Functions of the job:** + Management + Analysis + Strong Writing and communication skills + Working knowledge of statistical software such as SAS and R, MS office. + Ability to present posters and other oral presentations at the national and international congresses. **Education Required:** + PhD or equivalent, MA/MS/MPH or BA/BS **Qualifications:** + Ph.D. or an equivalent degree with proven records of PRO training, and 1 year plus experience in oncology COA, with related publications. + •BA/MS/MPH with 5 plus years experience in oncology COA strategy and PRO- related analysis, with related publications. + Skills in designs and product registration process. + Current knoeldge of the products in similar treatment land scape. + Ability to perform quick searches when needed, and work within tight dead-lines. **Computer Skills:** + MS office, Statistical analysis software (R and/or SAS) **Travel:** + 25% All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.