Support the design review and execution of RWE research projects using administrative claims data/ EMR including development of protocols contributing to statistical analysis plans (SAPs) reviewing and interpreting study results and abstract and manuscript development.
Stay current with research on RWE methodology and its applications as pertinent to project needs.
Oversee and manage study team communication project milestones dissemination of results to key members including internal and external collaborators.
Work collaboratively with members of study teams to meet study and recurring report timelines.
Minimum Requirements:
PhD in epidemiology (or similar area) with 2 years research experience or MS in epidemiology (or similar area) with 4 years research experience
At least 2 years with analytic experience of healthcare claims databases/EMR
Familiarity with US and global health care delivery system ( and reimbursement models)
Deep understanding of observational study design and analysis and ability to lead multi-disciplinary teams required to support program project and contract management and financial reporting
Experience designing and analyzing RWE from protocol development through public dissemination (e.g. abstracts and manuscripts)
Demonstrated strategic and conceptual skills to develop innovative approaches for developing product differentiation
Proficient in drug development regulations pertinent to RWE and in Oncology/Neuroscience therapeutic space
Able to work in a fast-paced flexible team-oriented environment.
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