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<http://schema.org/description>
"<p>IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers and patients. Our approach is unique in the industry and is defining the way companies can develop and apply real-world evidence to provide deeper insight about market dynamics, therapy area changes, outcomes research and other scientific insights. We are collaborative, intellectually curious, entrepreneurial and constantly looking for opportunities to harness the value of real-world evidence in a constantly evolving industry.</p><p></p><p>The most important role of an Analyst is to help in the project management of national and international non-interventional multi-country projects. Support in project management will often include liaising with other departments and geographies within IQVIA and managing sub-contractors.</p><p></p><p><b>Essential Responsibilities</b></p><ul><li><p>Assist on specific project or client management tasks under the supervision of a more senior colleague</p></li><li><p>Attend client and other external meetings in the home base country and elsewhere in Europe and the US, accompanied by a more senior colleague</p></li><li><p>Make oral presentations of own research / analysis to clients</p></li><li><p>Detect possible deviations or problems in study fieldwork and find best solution</p></li><li><p>Participate in customers and investigators meetings</p></li><li><p>Support in the administration control of the fees and expenses during the Project (travels, meetings, investigators payment).</p></li><li><p>Work within Quality Assurance SOP’s; follow up SOP’s, attend training, participate in internal and external audits, support SOP’s update to Quality Assurance</p></li><li><p>Support proposal development</p></li></ul><p></p><p><b>Required Experience and Skills</b></p><ul><li><p>Life sciences degree with at least 1 year relevant experience working in observational studies</p></li><li><p>Previous exposure of monitoring clinical trials ideal</p></li><li><p>Experience of working in sizable/multi-disciplined teams</p></li><li><p>Must be organized with strong capability in managing projects and juggling priorities so that deadlines are met while retaining consistently high quality outcomes</p></li><li><p>Excellent communication, written and verbal with strong client influencing skills</p></li><li><p>Good understanding of and interest in the international health care environment</p></li><li><p>Demonstrable analytical, interpretative and problem-solving skills</p></li><li><p>Flexible approach, prepared to adapt and reprioritize to meet clients and internal needs</p></li><li><p>You are a pro-active and stress resistant</p></li><li><p>You have an eye for detail and work accurately</p></li><li><p>Strong desire to learn new skills to meet business demands</p></li><li><p>High level of literacy – able to appraise evidence critically and write reports and manuscripts in clear, concise language as required by the type of work.</p></li><li><p>Good team-based interpersonal skills but also an ability to work independently.</p></li></ul><p></p><p>At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000&#43; employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at <a href='http://jobs.iqvia.com' target='_blank'>jobs.iqvia.com</a>.</p>"
<https://jobs.iqvia.com/job/barcelona/analyst-real-world-evidence/24443/14547313968>