.**BASIC FUNCTIONS**:The Associate Feasibility Manager is responsible for supporting the coordination and management of the efforts necessary for producing feasibility proposals and reports. In this capacity, this individual is responsible for assuring the Feasibility Associates and Analysts elicit input from and coordinate activities with all the stake holders in the feasibility process including: Proposals, Study Start-Up, Site Identification Services, Regulatory, Medical, IQVIA CORE, Project Management and Clinical Operations and combining resulting information with IQVIA Biotech's corporate experience to produce recommendations for country and site strategies. The Associate Feasibility Manager assures the assembly, editing, and review of feasibility proposals and reports, (feasibility proposals are documents that detail the strategy, actions, and the cost of conducting feasibility, and feasibility reports are documents that describe the outcomes of feasibility projects). The Associate Feasibility Manager may also participate in internal and external briefings and presentations of feasibility, when deemed necessary. This position reports directly to the Director of Feasibility in setting priorities for workload and deliverables in the department.The Associate Feasibility Manager continues to conduct clinical trial feasibility assessments based on Request for Proposals (RFPs).To conduct ad-hoc research as requested by IQVIA Biotech Clinical Sr. Management.**ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**:- Directs the activities of feasibility assessment and/or analysts under their direction.- Identifying and present regions where the disease is prominent to create an initial country pool to be further refined based on corporate experience, operational capabilities, medical input, and other feasibility considerations.- Identifying barriers to enrollment in the form of competing clinical trials. Accessing open source and proprietary databases to determine similar patient populations and or therapeutic classes of drugs being studied. Determine whether the countries proposed have comparator drug access/reimbursement. As appropriate prepare tabular displays of this information for evaluation by the feasibility stake holder pool.- Representing IQVIA Biotech's global or regional expertise by presenting our clinical trial footprint in the indication which may include compiling corporate experience and expertise in specific indication when needed.- Collaborating with IQVIA Biotech Regulatory Affairs determine regulatory timelines associated with the conduct of the proposed trial.- Work with the proposals team to determine costing of conducting a stand-alone feasibility assessment, if applicable.- Provides overall recommendations on the countries, number of sites and projected number of patients resulting from collaborative discussions noted above designed to meet or exceed client stated goals