Site Id and Feasibility Specialist

hace 3 semanas

Ciudad de México IQVIA A tiempo completo

**Job Overview**Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activitie. Developing professional individual contributor who works under moderate oversight and supervision. Responsible for making recommendations for enhancements in systems and processes to solve problems or improve effectiveness of job area. Problems faced are general and may require understanding of broader set of issues but are not complex.**Essential Functions**- Work with clinical study teams to ensure the accuracy of data in CTMS.- Provide support, under the direction of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist, to clinical systems end users, including receipt, evaluation and recommendation for all issue/enhancement requests.- Conduct research and data analysis to identify potential sites that meet the study criteria and objectives.- Assist with feasibility launch to include system set-up, feasibility questionnaire creation and site-level feasibility questionnaire outreach.- Effectively communicating with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities.- Tracking and data entry of feasibility responses and reporting responses to the internal stakeholders.- Troubleshoot any issues or discrepancies that arise in the feasibility process (in-house and/or outsourced studies).- Stay up-to-date with current regulations and industry trends related to site feasibility.**Qualifications**- Bachelor's Degree Life science or Scientific health field.- 3 years clinical research conducting clinical trials and processes, preferably with North America (sites).- 2 years of feasibility and recruitment.- Experience with trial optimization vendors, tools and methods.- Analytical thinker, attention to detail and good communication.- Highly proficient with excel.- Fluent Communication English.

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