Feasibility Specialist II - Contract

Purpose/ Summary: This position is for a contract opportunity. Facilitates the process of identifying site and investigator contacts for assigned feasibility projects that will meet internal and external client objectives. Operationally, source and analyze data to develop site/investigator targets and patient/therapeutic information for proposals and post-award feasibility offerings. Prepare and compile feasibility data and provide feasibility reports, create presentations to ensure the objective of the project is met. Ensure feasibility and investigator database are always up to date and cleaned on a regular basis by developing relationships with potential investigators and sites across multiple therapeutic area. What You'll Do: • Research, compile and analyze information on therapeutic area(s) to ensure proper feasibility target launch • Conduct research regarding disease incidence, prevalence, standard of care treatments, factors determining and influencing therapeutic indication frequency and distribution globally, treatment trends, competing trials, etc. • Perform database and literature search for site identification and identify and select sample sites • Design site surveys/questionnaires to obtain key information (e.g., investigator feedback on projected enrollment, feasibility of the study, and site capabilities) • Create surveys for data collection • Manage site information collection process and assess compiled information for trends and site capabilities • Collaborate with internal and site team members regarding survey completion • Create feasibility status reports for internal or external client use • Enter data and maintain existing data in, CTI feasibility and investigator data base to ensure information is up to date and still accurate. • Organize logistics and conduct feasibility calls with the sites • Create and deliver presentations and/or written reports, to internal/external stakeholders in the determined forum (e.g. client or team meeting) • Participate in intra- and inter-departmental meetings • Interact with internal and external sources to gather and share feasibility information • Provide input for proposals and business development to help build project assumptions, budgets, and timelines • Participate in strategy meetings with internal and external groups What You'll Bring: • Bachelor’s Degree in allied health field such as nursing, pharmacy or health science or the equivalent relevant experience • At least 2 years pharmaceutical or CRO Clinical Research experience About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com Apply tot his job