.Feasibility Study Specialist I (Please note this role can be located in any country where CTI has a legal entity) Job Purpose / Summary Assists in analyzing and researching institutions and Investigators via CTI Feasibility Database, Data Assets and Business Intelligence to develop site, investigator and patient information for business development proposals and post-award feasibility offerings. Responsibilities include assist with compiling feasibility reports, presentations, and sample site assessment for investigator feedback on study design and logistics, as well as enrollment potential, worldwide. This position reports directly to the Manager, Feasibility. What You'll Do Research and compile information on therapeutic area(s), collect information regarding incidence, prevalence, standard of care, factors determining and influencing indication frequency and distribution, treatment trends, competing trials, etc. Carry out database and literature search for sites identification. Assist in the identification/selection of potential sites and investigators and be able to present results to the internal team. Assist in the design of initial interest emails, site surveys/questionnaires to obtain key information (e.G., investigator feedback on projected enrollment, feasibility of the study, and site capabilities). Draft online survey (e.G., Survey Monkey) based on the approved questionnaire to facilitate the collection of data in the most efficient manner. Track responses of the online survey results and compile information for decision making. Ensure that feasibility tracking (Initial interest, CDA, survey completion, Feasibility teleconferences) and status updates are completed in real time and organize the information for review with the internal team and external client. Follow-up with internal team, sponsor and/or site staff regarding feasibility status. Enter information obtained into CTI feasibility database in order to ensure that the database is up to date at all times. Assist in the preparation, as applicable, of the feasibility call script for each site feasibility teleconference in order to ensure that all relevant and critical information will be obtained – review script with manager for approval. Organize all aspects of the feasibility calls with the sites in order to ensure that these calls run effectively. Assist in the preparation of presentations and/or written reports, as required, by summarizing the relevant information and discussing within the team in order to present to sponsor and obtain next step approval. Participates in intra- and inter-departmental meetings including kick-off meetings as well as sponsor meetings. What You'll Bring High School Graduate. 0-1 years pharmaceutical or CRO Clinical Research experience. Excellent verbal and written communication skills. Excellent organizational, time and personal management skills. Good data analytic skills. Good creative problem-solving skills
